Yeast Systematic Name | Yeast Symbol | SGDID | Analog Name | Analog Description | EC | Organism | Disease | Structure | Uniprot | Human ID | Human Symbol | HHsearch Probability | HHsearch E_value | HHsearch P_value | HHsearch Score | Flag Disease related | Flag Homo sapiens | Flag Mus musculus | Flag Danio rerio | Flag Drosophila melanogaster | Flag Caenorhabditis elegans | Flag Arabidopsis thaliana | Flag Escherichia coli |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YNL154C | YCK2 | SGDID:S000005098 | CSNK1G3 |
Casein kinase I isoform gamma-3 (CKI-gamma 3) (EC 2.7.11.1) |
2.7.11.1 | Homo sapiens | 2izr_a | Q9Y6M4 | ENSG00000151292 | CSNK1G3 | 99.70 | 8.80E-23 | 9.90E-27 | 195.60 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YNL154C | YCK2 | SGDID:S000005098 | TCM_042446 |
TCM_042446 |
Theobroma cacao | 6cth_a | A0A061FLD4 | 98.90 | 1.90E-13 | 2.20E-17 | 126.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YNL154C | YCK2 | SGDID:S000005098 | RET CDHF12 CDHR16 PTC RET51 |
Proto-oncogene tyrosine-protein kinase receptor Ret (EC 2.7.10.1) (Cadherin family member 12) (Proto-oncogene c-Ret) [Cleaved into: Soluble RET kinase fragment; Extracellular cell-membrane anchored RET cadherin 120 kDa fragment] |
2.7.10.1 | Homo sapiens | Spitzoid Melanoma,Megacolon,Neuroendocrine Tumor,Endocrine Gland Cancer,Endometrial Cancer,Intestinal Pseudo-Obstruction,Follicular Adenoma,Retinitis Pigmentosa,Thyroid Gland Cancer,Islet Cell Tumor,Amyloidosis,Renal Hypoplasia,Cakut,Achalasia,Medullary Sponge Kidney,Cowden Syndrome,Solid Adenocarcinoma With Mucin Production,Peripheral Nervous System Benign Neoplasm,Autonomic Nervous System Benign Neoplasm,Waardenburg'S Syndrome,Rare Tumor,Lung Non-Squamous Non-Small Cell Carcinoma,Thyroid Gland Anaplastic Carcinoma,Adenoma,Parathyroid Carcinoma,Sporadic Pheochromocytoma/Secreting Paraganglioma,Primary Peritoneal Carcinoma,Neuronal Intestinal Dysplasia, Type B,B-Lymphoblastic Leukemia/Lymphoma,Neuroma,B-Lymphoblastic Leukemia/Lymphoma With Hypodiploidy,Constipation,Esophagus Leiomyoma,Multicentric Papillary Thyroid Carcinoma,Tall Cell Variant Papillary Carcinoma,Goiter,Thyroiditis,Differentiated Thyroid Carcinoma,Motor Neuron Disease,Neurofibromatosis, Type I,Parathyroid Adenoma,Ganglioneuroma,Lymph Node Disease,Neuroblastoma,Multiple Endocrine Neoplasia, Type Iib,Pilocytic Astrocytoma,Inherited Cancer-Predisposing Syndrome,Hypertrophic Pyloric Stenosis,Testicular Spermatocytic Seminoma,Pyloric Stenosis,Hemangioma,Thyroid Gland Disease,Central Nervous System Hemangioma,Atypical Follicular Adenoma,Carney Complex Variant,Intestinal Obstruction,Struma Ovarii,Multiple Mucosal Neuroma,Pheochromocytoma-Paraganglioma,Hypoganglionosis,Sudden Infant Death Syndrome,Sensorineural Hearing Loss,Malignant Struma Ovarii,Benign Struma Ovarii,Thyroid Carcinoma,Hereditary Paraganglioma-Pheochromocytoma Syndromes,Thyroid Tumor,Hypermobile Ehlers-Danlos Syndrome,Lung Disease,Gingival Hypertrophy,Nodular Goiter,Skin Lipoma,Lichen Amyloidosis,Ovarian Germ Cell Teratoma,Primary Hyperoxaluria,Kidney Disease,Adenocarcinoma,Neurofibromatosis,Hyperparathyroidism,Charcot-Marie-Tooth Disease,Breast Cancer,Renal Agenesis, Bilateral,Adrenal Medulla Cancer,Colorectal Cancer,Gingival Overgrowth,Papillary Carcinoma,Multiple Endocrine Neoplasia,Nonencapsulated Sclerosing Carcinoma,Microcephaly,Pheochromocytoma,Goldberg-Shprintzen Syndrome,Multiple Endocrine Neoplasia, Type Iia,Tooth Disease,Waardenburg Syndrome, Type 4a,Renal Hypodysplasia/Aplasia 3,Hypoparathyroidism,Parathyroid Gland Disease,Primary Hyperparathyroidism,Hypothyroidism,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Multiple Endocrine Neoplasia, Type Iv,Lung Squamous Cell Carcinoma,Thyroid Gland Follicular Carcinoma,Thyroid Gland Medullary Carcinoma,Multiple Endocrine Neoplasia, Type I,Tetralogy Of Fallot,Alveolar Soft Part Sarcoma,Tumor Predisposition Syndrome,Autosomal Genetic Disease,Ewing Sarcoma,Paraganglioma,Hashimoto Thyroiditis,Renal Hypodysplasia/Aplasia 1,Hirschsprung Disease 1,Paraganglioma And Gastric Stromal Sarcoma,Vesicoureteral Reflux 1,Von Hippel-Lindau Syndrome,Parkinson Disease 8, Autosomal Dominant,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Renal Cell Carcinoma, Nonpapillary,Extra-Adrenal Pheochromocytoma,Hypertelorism,Autoimmune Disease Of Endocrine System,Meningioma, Familial,Endocrine Organ Benign Neoplasm,Cardiovascular Organ Benign Neoplasm,Persistent Generalized Lymphadenopathy,Thyroid Carcinoma, Familial Medullary,Medulloblastoma,Central Hypoventilation Syndrome, Congenital,Familial Hypocalciuric Hypercalcemia,Lung Cancer,Pancreatic Cancer |
4ckj_a | P07949 | ENSG00000165731 | RET | 98.90 | 1.30E-13 | 1.60E-17 | 126.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | EPHA2 ECK |
Ephrin type-A receptor 2 (EC 2.7.10.1) (Epithelial cell kinase) (Tyrosine-protein kinase receptor ECK) |
2.7.10.1 | Homo sapiens | Pancreatic Adenocarcinoma,Melanoma,Senile Cataract,Early-Onset Posterior Subcapsular Cataract,Gliofibroma,Early-Onset Nuclear Cataract,Early-Onset Posterior Polar Cataract,Cataract,Glanders,Ovarian Cancer,Pendred Syndrome,Adenocarcinoma,Cortical Senile Cataract,Breast Cancer,Glioblastoma,Colorectal Cancer,Early-Onset Non-Syndromic Cataract,Cataract 7,Hepatitis C Virus,Cataract 6, Multiple Types,Prostate Cancer,Gastric Adenocarcinoma,Lung Squamous Cell Carcinoma,Posterior Polar Cataract,Ewing Sarcoma,Renal Cell Carcinoma, Nonpapillary,Cataract 44,Lung Cancer |
5nkh_a | P29317 | ENSG00000142627 | EPHA2 | 98.90 | 1.70E-13 | 2.10E-17 | 125.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | DDR1 CAK EDDR1 NEP NTRK4 PTK3A RTK6 TRKE |
Epithelial discoidin domain-containing receptor 1 (Epithelial discoidin domain receptor 1) (EC 2.7.10.1) (CD167 antigen-like family member A) (Cell adhesion kinase) (Discoidin receptor tyrosine kinase) (HGK2) (Mammary carcinoma kinase 10) (MCK-10) (Protein-tyrosine kinase 3A) (Protein-tyrosine kinase RTK-6) (TRK E) (Tyrosine kinase DDR) (Tyrosine-protein kinase CAK) (CD antigen CD167a) |
2.7.10.1 | Homo sapiens | Cervix Small Cell Carcinoma,Meninges Sarcoma,Breast Cancer,Alport Syndrome,Pulmonary Fibrosis, Idiopathic,Lymphangioleiomyomatosis |
6fex_a | Q08345 | ENSG00000204580 | DDR1 | 98.90 | 1.50E-13 | 1.70E-17 | 127.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | MYLK4 SGK085 |
Myosin light chain kinase family member 4 (EC 2.7.11.1) (Sugen kinase 85) (SgK085) |
2.7.11.1 | Homo sapiens | Cardiomyopathy, Familial Restrictive, 2,Deafness, Autosomal Recessive 17,Deafness, Autosomal Recessive 14,Cardiomyopathy, Familial Restrictive, 3 |
2x4f_a | Q86YV6 | ENSG00000145949 | MYLK4 | 98.90 | 1.10E-13 | 1.20E-17 | 133.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | MAP3K14 NIK |
Mitogen-activated protein kinase kinase kinase 14 (EC 2.7.11.25) (NF-kappa-beta-inducing kinase) (HsNIK) (Serine/threonine-protein kinase NIK) |
2.7.11.25 | Homo sapiens | T-Cell Lymphoblastic Leukemia/Lymphoma,Nik Deficiency,Trichohepatoenteric Syndrome 1,Pancreatic Adenosquamous Carcinoma,Pancreatic Ductal Adenocarcinoma,Immunodeficiency 50 |
4idv_c | Q99558 | ENSG00000006062 | MAP3K14 | 99.10 | 9.20E-15 | 1.10E-18 | 138.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | CDKL5 STK9 |
Cyclin-dependent kinase-like 5 (EC 2.7.11.22) (Serine/threonine-protein kinase 9) |
2.7.11.22 | Homo sapiens | Cdkl5 Deficiency Disorder,Ohtahara Syndrome,Seizure Disorder,Childhood Absence Epilepsy,Epilepsy,Gait Apraxia,Gene Duplication Disease,Nicolaides-Baraitser Syndrome,Amyotrophic Lateral Sclerosis 1,Angelman Syndrome,Focal Epilepsy,Developmental And Epileptic Encephalopathy 14,Epilepsy With Generalized Tonic-Clonic Seizures,Congenital Nervous System Abnormality,Developmental And Epileptic Encephalopathy,Fundus Dystrophy,Juvenile Retinoschisis,Bruxism,X-Linked Congenital Retinoschisis,Early Myoclonic Encephalopathy,Stxbp1 Encephalopathy,Microcephaly,Mental Retardation, Autosomal Dominant 20,Encephalopathy,Benign Neonatal Seizures,Alacrima, Achalasia, And Mental Retardation Syndrome,Benign Epilepsy With Centrotemporal Spikes,Developmental And Epileptic Encephalopathy 9,Methylmalonic Acidemia,Benign Familial Neonatal Epilepsy,West Syndrome,Disease Of Mental Health,Lubs X-Linked Mental Retardation Syndrome,Fragile X Syndrome,Pitt-Hopkins Syndrome,Mowat-Wilson Syndrome,Developmental And Epileptic Encephalopathy 2,Lennox-Gastaut Syndrome,Sturge-Weber Syndrome,Neonatal Period Electroclinical Syndrome,Infancy Electroclinical Syndrome,Childhood Electroclinical Syndrome,Early Infantile Epileptic Encephalopathy,Developmental And Epileptic Encephalopathy 4,Myasthenic Syndrome, Congenital, 11, Associated With Acetylcholine Receptor Deficiency,Encephalopathy Due To Defective Mitochondrial And Peroxisomal Fission 1,Aicardi Syndrome,Specific Developmental Disorder,Pervasive Developmental Disorder,Dravet Syndrome,Developmental And Epileptic Encephalopathy 1,Benign Familial Infantile Epilepsy,Generalized Epilepsy With Febrile Seizures Plus,Pyruvate Dehydrogenase E1-Alpha Deficiency,Retinoschisis 1, X-Linked, Juvenile,Rett Syndrome,Epilepsy, Myoclonic Juvenile,Autism,Christianson Syndrome,Epilepsy, Idiopathic Generalized,Peho Syndrome |
4bgq_a | O76039 | ENSG00000008086 | CDKL5 | 99.00 | 7.10E-14 | 8.60E-18 | 126.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | PHKG2 |
Phosphorylase b kinase gamma catalytic chain, liver/testis isoform (PHK-gamma-LT) (PHK-gamma-T) (EC 2.7.11.19) (PSK-C3) (Phosphorylase kinase subunit gamma-2) |
2.7.11.19 | Homo sapiens | Glycogen Storage Disease Ixa,Glycogen Storage Disease Ixc,Glycogen Storage Disease,Phosphorylase Kinase Deficiency,Glycogen Storage Disease Due To Liver Phosphorylase Kinase Deficiency,Glycogen Storage Disease Ia,Glycogen Storage Disease, Type Ixd,Glycogen Storage Disease Ix,Glycogen Storage Disease Ixb |
2y7j_c | P15735 | ENSG00000156873 | PHKG2 | 98.90 | 3.40E-13 | 3.90E-17 | 128.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | LIMK1 LIMK |
LIM domain kinase 1 (LIMK-1) (EC 2.7.11.1) |
2.7.11.1 | Homo sapiens | Breast Cancer,Intracranial Aneurysm,Prostate Cancer,Disease Of Mental Health,Fragile X Syndrome,Supravalvular Aortic Stenosis,Williams-Beuren Syndrome,Polycystic Kidney Disease 3 With Or Without Polycystic Liver Disease |
3s95_b | P53667 | ENSG00000106683 | LIMK1 | 99.10 | 5.10E-15 | 6.10E-19 | 136.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | PTK2B FAK2 PYK2 RAFTK |
Protein-tyrosine kinase 2-beta (EC 2.7.10.2) (Calcium-dependent tyrosine kinase) (CADTK) (Calcium-regulated non-receptor proline-rich tyrosine kinase) (Cell adhesion kinase beta) (CAK-beta) (CAKB) (Focal adhesion kinase 2) (FADK 2) (Proline-rich tyrosine kinase 2) (Related adhesion focal tyrosine kinase) (RAFTK) |
2.7.10.2 | Homo sapiens | Leukemia, Chronic Myeloid,Transient Cerebral Ischemia,Retinal Degeneration,Mixed Cell Adenoma,Osteoporosis,Ovarian Cancer,Osteopetrosis,Breast Cancer,Hepatocellular Carcinoma,Prostate Cancer,Disease Of Mental Health,Lung Cancer |
3cc6_a | Q14289 | ENSG00000120899 | PTK2B | 98.90 | 1.10E-13 | 1.30E-17 | 124.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | Map3k14 Nik |
Mitogen-activated protein kinase kinase kinase 14 (EC 2.7.11.25) (NF-kappa-beta-inducing kinase) (Serine/threonine-protein kinase NIK) |
2.7.11.25 | Mus musculus | 4g3f_a | Q9WUL6 | 99.00 | 2.40E-14 | 2.80E-18 | 134.20 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YNL154C | YCK2 | SGDID:S000005098 | PRKCB PKCB PRKCB1 |
Protein kinase C beta type (PKC-B) (PKC-beta) (EC 2.7.11.13) |
2.7.11.13 | Homo sapiens | Severe Nonproliferative Diabetic Retinopathy,Hyperglycemia,Macroglobulinemia,Diabetic Macular Edema,Microvascular Complications Of Diabetes 5,Diabetes Mellitus,Macular Retinal Edema,B-Cell Lymphoma,Myotonic Dystrophy 1,Primary Biliary Cholangitis,Diabetic Neuropathy,Kidney Disease,Eye Disease,Glioblastoma,Hepatocellular Carcinoma,Type 2 Diabetes Mellitus,Leukemia, Chronic Lymphocytic,Autism,Lung Cancer |
2i0e_a | P05771 | ENSG00000166501 | PRKCB | 98.90 | 1.40E-13 | 1.60E-17 | 130.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | let-23 kin-7 ZK1067.1 |
Receptor tyrosine-protein kinase let-23 (EC 2.7.10.1) (Lethal protein 23) |
2.7.10.1 | Caenorhabditis elegans | 5wno_a | P24348 | 98.90 | 1.80E-13 | 2.00E-17 | 128.50 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | |||
YNL154C | YCK2 | SGDID:S000005098 | BTK AGMX1 ATK BPK |
Tyrosine-protein kinase BTK (EC 2.7.10.2) (Agammaglobulinemia tyrosine kinase) (ATK) (B-cell progenitor kinase) (BPK) (Bruton tyrosine kinase) |
2.7.10.2 | Homo sapiens | Pneumocystosis,X-Linked Recessive Disease,Lymphopenia,Conjunctivitis,Richter'S Syndrome,Macroglobulinemia,Pyoderma,Cll/Sll,Mast-Cell Leukemia,Polyarticular Juvenile Idiopathic Arthritis,Spherocytosis, Type 5,Ecthyma,B Cell Deficiency,Lung Large Cell Carcinoma,B-Cell Lymphoma,Common Variable Immunodeficiency,Neutropenia,Agammaglobulinemia 1, Autosomal Recessive,Plasma Protein Metabolism Disease,Isolated Agammaglobulinemia,Poliomyelitis,Leukemia, Acute Myeloid,Growth Hormone Deficiency,Leukemia, Acute Lymphoblastic,Agammaglobulinemia,Bacterial Infectious Disease,Breast Cancer,Central Nervous System Hematologic Cancer,Congenital Hypogammaglobulinemia,Immunodeficiency 14,Panniculitis,Immunodeficiency 33,Lymphoma, Non-Hodgkin, Familial,Baylisascariasis,Agammaglobulinemia, X-Linked,Paralytic Poliomyelitis,Immune Deficiency Disease,Myelodysplastic Syndrome,Immunoglobulin A Deficiency 1,Wiskott-Aldrich Syndrome,X-Linked Monogenic Disease,Diffuse Large B-Cell Lymphoma,Mantle Cell Lymphoma,Lymphoplasmacytic Lymphoma,Marginal Zone B-Cell Lymphoma,Splenic Marginal Zone Lymphoma,Williams-Beuren Syndrome,Combined Oxidative Phosphorylation Deficiency 9,Mohr-Tranebjaerg Syndrome,Cd40 Ligand Deficiency,Isolated Growth Hormone Deficiency, Type Iii, With Agammaglobulinemia,Immunodeficiency 45,Immunodeficiency With Hyper-Igm, Type 1,Leukemia, Chronic Lymphocytic,Myeloma, Multiple,Isolated Growth Hormone Deficiency,Isolated Growth Hormone Deficiency Type Iii,Waldenstroem'S Macroglobulinemia |
5p9j_a | Q06187 | ENSG00000010671 | BTK | 99.10 | 1.50E-14 | 1.80E-18 | 130.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | KSR2 |
Kinase suppressor of Ras 2 (hKSR2) (EC 2.7.11.1) |
Homo sapiens | 5kkr_b | Q6VAB6 | ENSG00000171435 | KSR2 | 98.90 | 9.10E-14 | 1.10E-17 | 127.80 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YNL154C | YCK2 | SGDID:S000005098 | PBL2 APK2A KIN1 At1g14370 F14L17.14 |
Probable serine/threonine-protein kinase PBL2 (EC 2.7.11.1) (PBS1-like protein 2) (Protein kinase 2A) |
2.7.11.1 | Arabidopsis thaliana | 6j5t_d | O49839 | 99.00 | 6.10E-14 | 6.90E-18 | 137.30 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
YNL154C | YCK2 | SGDID:S000005098 | SRC SRC1 |
Proto-oncogene tyrosine-protein kinase Src (EC 2.7.10.2) (Proto-oncogene c-Src) (pp60c-src) (p60-Src) |
2.7.10.2 | Homo sapiens | Pancreatic Adenocarcinoma,Bone Disease,Skin Melanoma,Differentiating Neuroblastoma,Cryptococcal Meningitis,Retinitis Pigmentosa,Myeloid And Lymphoid Neoplasms Associated With Fgfr1 Abnormalities,Lung Cancer Susceptibility 3,Myopathy,Polycystic Kidney Disease,Leukemia, Chronic Myeloid,Gastroesophageal Adenocarcinoma,Bone Sarcoma,Hepatitis B,Rasopathy,Avian Influenza,Myocardial Infarction,Teeth Hard Tissue Disease,Amelogenesis Imperfecta,Essential Thrombocythemia,Neuroblastoma,Leukemia, Acute Myeloid,Cystic Fibrosis,Bone Marrow Cancer,Leukemia, Acute Lymphoblastic,Agammaglobulinemia,Autonomic Nervous System Neoplasm,Bladder Cancer,Osteoporosis,Ovarian Cancer,Pylorus Cancer,Osteopetrosis,Breast Cancer,Glioblastoma,Squamous Cell Carcinoma, Head And Neck,Diamond-Blackfan Anemia 10,Anaplastic Astrocytoma,Colorectal Cancer,Peripheral Nervous System Disease,Hepatocellular Carcinoma,Human Immunodeficiency Virus Type 1,Noonan Syndrome With Multiple Lentigines,Alzheimer Disease 11,Cherubism,Sarcoma,Skin Carcinoma,Cone-Rod Dystrophy 2,Alzheimer Disease 18,Tetanus,Prostate Cancer,Disease Of Mental Health,Signet Ring Cell Adenocarcinoma,Body Mass Index Quantitative Trait Locus 11,Thrombocytopenia,Lynch Syndrome,Lung Squamous Cell Carcinoma,Agammaglobulinemia, X-Linked,Hypotrichosis 1,Wiskott-Aldrich Syndrome,Maturity-Onset Diabetes Of The Young,Acute Promyelocytic Leukemia,Pulmonary Disease, Chronic Obstructive,Hypertension, Essential,Meningioma, Familial,Frank-Ter Haar Syndrome,Estrogen-Receptor Positive Breast Cancer,Estrogen-Receptor Negative Breast Cancer,Coenzyme Q10 Deficiency, Primary, 1,Amelogenesis Imperfecta, Type Ig,Thrombocytopenia 6,Myelofibrosis,Myeloma, Multiple,Medulloblastoma,Lung Cancer,Pancreatic Cancer,Polycythemia Vera |
1y57_a | P12931 | ENSG00000197122 | SRC | 99.10 | 1.60E-14 | 1.90E-18 | 140.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | CSNK1D HCKID |
Casein kinase I isoform delta (CKI-delta) (CKId) (EC 2.7.11.1) (Tau-protein kinase CSNK1D) (EC 2.7.11.26) |
2.7.11.1,2.7.11.26, | Homo sapiens | Migraine With Or Without Aura 1,Alzheimer Disease,Sleep Disorder,Advanced Sleep Phase Syndrome, Familial, 2,Breast Cancer,Disease Of Mental Health,Delayed Sleep Phase Disorder,Advanced Sleep Phase Syndrome |
4kb8_b | P48730 | ENSG00000141551 | CSNK1D | 99.40 | 1.20E-17 | 1.40E-21 | 157.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | RIPK1 RIP RIP1 |
Receptor-interacting serine/threonine-protein kinase 1 (EC 2.7.11.1) (Cell death protein RIP) (Receptor-interacting protein 1) (RIP-1) |
2.7.11.1 | Homo sapiens | Inflammatory Bowel Disease 25, Autosomal Recessive,Zika Virus Congenital Syndrome,Autoinflammation, Panniculitis, And Dermatosis Syndrome,Cutaneous Diphtheria,Arthritis,Autoimmune Lymphoproliferative Syndrome,Mumps,Immunodeficiency 57 With Autoinflammation,Inflammatory Bowel Disease,Immune Deficiency Disease,Caspase 8 Deficiency,Incontinentia Pigmenti,Autoinflammation With Episodic Fever And Lymphadenopathy,Gordon Holmes Syndrome |
4itj_b | Q13546 | ENSG00000137275 | RIPK1 | 98.90 | 1.70E-13 | 2.10E-17 | 122.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | TTN |
Titin (EC 2.7.11.1) (Connectin) (Rhabdomyosarcoma antigen MU-RMS-40.14) |
2.7.11.1 | Homo sapiens | Muscular Disease,Heart Disease,Constrictive Pericarditis,Congenital Fiber-Type Disproportion,Mitral Valve Insufficiency,Aortic Valve Disease 2,Congenital Structural Myopathy,Myopathy,Amyloidosis,Cardiomyopathy, Dilated, 1e,Syncope,Myofibrillar Myopathy,Atrial Heart Septal Defect,Mitochondrial Dna Depletion Syndrome 12b,Childhood-Onset Progressive Contractures-Limb-Girdle Weakness-Muscle Dystrophy Syndrome,Emery-Dreifuss Muscular Dystrophy,Cortical Thymoma,Muscle Tissue Disease,Morvan'S Fibrillary Chorea,Neuromuscular Disease,Hypertrophic Cardiomyopathy,Familial Isolated Dilated Cardiomyopathy,Rasopathy,Autosomal Dominant Distal Myopathy,Lung Large Cell Carcinoma,Myopathy, Distal, 1,Myositis,Myotonic Dystrophy 1,Systolic Heart Failure,Myopathy, Myofibrillar, 1,Diastolic Heart Failure,Autosomal Recessive Limb-Girdle Muscular Dystrophy,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2a,Muscular Dystrophy,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2g,Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2j,Muscular Atrophy,Tibial Muscular Dystrophy,Limb-Girdle Muscular Dystrophy,Arrhythmogenic Right Ventricular Dysplasia, Familial, 1,Epithelial Malignant Thymoma,Hyaline Body Myopathy,Isolated Elevated Serum Creatine Phosphokinase Levels,Noonan Syndrome 1,Newborn Respiratory Distress Syndrome,Thymus Clear Cell Carcinoma,Reducing Body Myopathy,Myocarditis,Atrial Standstill 1,Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 10,Hereditary Proximal Myopathy With Early Respiratory Failure,Dilated Cardiomyopathy,Alcoholic Cardiomyopathy,Lmna-Related Dilated Cardiomyopathy,Thymus Gland Disease,Long Qt Syndrome,Cardiomyopathy, Dilated, 1dd,Heart Conduction Disease,Udd Distal Myopathy - Tibial Muscular Dystrophy,Muscular Dystrophy, Congenital, Lmna-Related,Neuropathy,Perinephritis,Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form,Familial Isolated Arrhythmogenic Ventricular Dysplasia, Biventricular Form,Familial Isolated Arrhythmogenic Ventricular Dysplasia, Left Dominant Form,Myopathy, Myofibrillar, 3,Sick Sinus Syndrome,Multiminicore Disease,Cardiomyopathy, Familial Hypertrophic, 4,Cardiomyopathy, Dilated, 1a,Congestive Heart Failure,Myopathy, Myofibrillar, 4,Left Ventricular Noncompaction 2,Foot Drop,Myopathy, Myofibrillar, 5,Rhabdomyosarcoma,Rigid Spine Muscular Dystrophy 1,Epidermolysis Bullosa Simplex With Muscular Dystrophy,Thymoma,Thymus Cancer,Dendritic Cell Thymoma,Respiratory Failure,Centronuclear Myopathy,Myopathy, Myofibrillar, 9, With Early Respiratory Failure,Cardiomyopathy, Dilated, 1g,Congenital Myasthenic Syndrome,Cardiomyopathy, Familial Hypertrophic, 9,Cardiomyopathy, Dilated, 1h,Orthostatic Intolerance,Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant,Lung Squamous Cell Carcinoma,Restrictive Cardiomyopathy,Extrinsic Cardiomyopathy,Lambert-Eaton Myasthenic Syndrome,Arrhythmogenic Right Ventricular Cardiomyopathy,Brugada Syndrome,Muscle Hypertrophy,Salih Myopathy,Nonaka Myopathy,Primary Cutaneous Amyloidosis,Distal Arthrogryposis,Familial Atrial Fibrillation,Hypermethioninemia Due To Adenosine Kinase Deficiency,Atrioventricular Block,Third-Degree Atrioventricular Block,Barth Syndrome,Cardioneuromyopathy With Hyaline Masses And Nemaline Rods,Cardiomyopathy, Familial Hypertrophic, 1,Wolff-Parkinson-White Syndrome,Muscular Dystrophy-Dystroglycanopathy , Type C, 5,Intrinsic Cardiomyopathy,Peripartum Cardiomyopathy,Lipoprotein Quantitative Trait Locus,Atrial Fibrillation,Scoliosis,Muscular Dystrophy, Duchenne Type,Myopathy, Centronuclear, X-Linked,Cardiac Arrest,Inguinal Hernia,Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2,Myasthenia Gravis,Left Ventricular Noncompaction,Lethal Congenital Contracture Syndrome,Myopathy, Centronuclear, 2,Batten-Turner Congenital Myopathy,Miyoshi Muscular Dystrophy,Tibial Muscular Dystrophy, Tardive,Cardiomyopathy, Dilated, 1b |
1tki_b | Q8WZ42 | ENSG00000155657 | TTN | 98.90 | 1.40E-13 | 1.70E-17 | 128.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | EIF2AK3 PEK PERK |
Eukaryotic translation initiation factor 2-alpha kinase 3 (EC 2.7.11.1) (PRKR-like endoplasmic reticulum kinase) (Pancreatic eIF2-alpha kinase) (HsPEK) |
2.7.11.1 | Homo sapiens | Skin Melanoma,Retinitis Pigmentosa,Neonatal Diabetes,Prion Disease,Diabetes Mellitus,Alzheimer Disease,Rasopathy,Retinal Degeneration,Subungual Glomus Tumor,Crisponi/Cold-Induced Sweating Syndrome 1,Osteoporosis,Wolfram Syndrome,Epiphyseal Dysplasia, Multiple, With Early-Onset Diabetes Mellitus,Disease Of Mental Health,Leukoencephalopathy With Vanishing White Matter,Odontochondrodysplasia,Trichothiodystrophy 5, Nonphotosensitive,Cardiomyopathy, Familial Hypertrophic, 25,Permanent Neonatal Diabetes Mellitus,Palmoplantar Keratoderma, Bothnian Type |
4x7k_a | Q9NZJ5 | ENSG00000172071 | EIF2AK3 | 98.90 | 2.40E-13 | 2.90E-17 | 124.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | SRC |
Proto-oncogene tyrosine-protein kinase Src (EC 2.7.10.2) (Proto-oncogene c-Src) (pp60c-src) (p60-Src) |
2.7.10.2 | Gallus gallus | 3u4w_a | P00523 | 99.20 | 2.20E-15 | 2.60E-19 | 135.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YNL154C | YCK2 | SGDID:S000005098 | YCK1 CKI2 YHR135C |
Casein kinase I homolog 1 (EC 2.7.11.1) |
2.7.11.1 | Saccharomyces cerevisiae | 5x18_b | P23291 | 99.90 | 2.00E-30 | 2.40E-34 | 241.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YNL154C | YCK2 | SGDID:S000005098 | ROR2 NTRKR2 |
Tyrosine-protein kinase transmembrane receptor ROR2 (EC 2.7.10.1) (Neurotrophic tyrosine kinase, receptor-related 2) |
2.7.10.1 | Homo sapiens | Robinow Syndrome, Autosomal Recessive 1,Autosomal Dominant Robinow Syndrome,Basal Cell Nevus Syndrome,Brachydactyly, Type A1,Ror2-Related Robinow Syndrome,Brachydactyly, Type B1,Fallopian Tube Serous Adenocarcinoma,Breast Cancer,Polydactyly,Robinow Syndrome, Autosomal Dominant 1,Brachydactyly,Distal Arthrogryposis,Proximal Symphalangism,Robinow Syndrome,Omodysplasia,Fetal Akinesia Deformation Sequence 1 |
3zzw_a | Q01974 | ENSG00000169071 | ROR2 | 98.90 | 2.40E-13 | 3.00E-17 | 120.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | TNNI3K CARK |
Serine/threonine-protein kinase TNNI3K (EC 2.7.11.1) (Cardiac ankyrin repeat kinase) (Cardiac troponin I-interacting kinase) (TNNI3-interacting kinase) |
2.7.11.1 | Homo sapiens | Dilated Cardiomyopathy,Restrictive Cardiomyopathy,Cardiac Conduction Disease With Or Without Dilated Cardiomyopathy,Familial Atrial Fibrillation |
4yfi_a | Q59H18 | ENSG00000259030 | FPGT-TNNI3K | 99.10 | 4.40E-15 | 5.40E-19 | 137.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | RIPK2 CARDIAK RICK RIP2 UNQ277/PRO314/PRO34092 |
Receptor-interacting serine/threonine-protein kinase 2 (EC 2.7.11.1) (CARD-containing interleukin-1 beta-converting enzyme-associated kinase) (CARD-containing IL-1 beta ICE-kinase) (RIP-like-interacting CLARP kinase) (Receptor-interacting protein 2) (RIP-2) (Tyrosine-protein kinase RIPK2) (EC 2.7.10.2) |
2.7.10.2,2.7.11.1, | Homo sapiens | Inflammatory Bowel Disease 1,Indeterminate Leprosy,Ulnar Nerve Lesion,Radial Nerve Lesion,Testicular Disease,Crohn'S Disease,Human Granulocytic Anaplasmosis,Lymphoproliferative Syndrome, X-Linked, 2,Inflammatory Bowel Disease,Blau Syndrome,Chromosome 8q21.11 Deletion Syndrome,Leprosy 3 |
5ng0_a | O43353 | ENSG00000104312 | RIPK2 | 98.90 | 1.60E-13 | 1.90E-17 | 124.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | HCK |
Tyrosine-protein kinase HCK (EC 2.7.10.2) (Hematopoietic cell kinase) (Hemopoietic cell kinase) (p59-HCK/p60-HCK) (p59Hck) (p61Hck) |
2.7.10.2 | Homo sapiens | Leukemia, Chronic Myeloid,Tinea Favosa,Renal Pelvis Adenocarcinoma,Leukemia, Acute Lymphoblastic,Human Immunodeficiency Virus Type 1,Co-Trimoxazole Allergy,Immune Deficiency Disease |
2hck_b | P08631 | ENSG00000101336 | HCK | 99.00 | 2.80E-14 | 3.30E-18 | 138.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | Btk Bpk |
Tyrosine-protein kinase BTK (EC 2.7.10.2) (Agammaglobulinemia tyrosine kinase) (ATK) (B-cell progenitor kinase) (BPK) (Bruton tyrosine kinase) (Kinase EMB) |
2.7.10.2 | Mus musculus | 4xi2_a | P35991 | 99.00 | 5.20E-14 | 6.00E-18 | 137.30 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YNL154C | YCK2 | SGDID:S000005098 | STK4 KRS2 MST1 |
Serine/threonine-protein kinase 4 (EC 2.7.11.1) (Mammalian STE20-like protein kinase 1) (MST-1) (STE20-like kinase MST1) (Serine/threonine-protein kinase Krs-2) [Cleaved into: Serine/threonine-protein kinase 4 37kDa subunit (MST1/N); Serine/threonine-protein kinase 4 18kDa subunit (MST1/C)] |
2.7.11.1 | Homo sapiens | T-Cell Immunodeficiency, Recurrent Infections, And Autoimmunity With Or Without Cardiac Malformations,Myeloproliferative Syndrome, Transient,Lymphoproliferative Syndrome 2,Epidermodysplasia Verruciformis 1,Immunodeficiency 13,Prostate Cancer,Coronin-1a Deficiency,Wilson-Turner X-Linked Mental Retardation Syndrome,Lung Cancer |
3com_a | Q13043 | ENSG00000101109 | STK4 | 98.90 | 1.80E-13 | 2.10E-17 | 126.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | P0510F09.27 |
P0510F09.27 |
Oryza sativa | 3sv0_a | Q8LR51 | 99.50 | 1.50E-18 | 1.60E-22 | 178.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YNL154C | YCK2 | SGDID:S000005098 | CSNK1G1 |
Casein kinase I isoform gamma-1 (CKI-gamma 1) (EC 2.7.11.1) |
2.7.11.1 | Homo sapiens | Epilepsy,Epilepsy With Generalized Tonic-Clonic Seizures,Aortic Valve Prolapse,Gm1-Gangliosidosis, Type I,Gm1-Gangliosidosis, Type Ii |
2cmw_a | Q9HCP0 | ENSG00000169118 | CSNK1G1 | 99.50 | 4.40E-19 | 5.30E-23 | 162.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | ABL1 ABL JTK7 |
Tyrosine-protein kinase ABL1 (EC 2.7.10.2) (Abelson murine leukemia viral oncogene homolog 1) (Abelson tyrosine-protein kinase 1) (Proto-oncogene c-Abl) (p150) |
2.7.10.2 | Homo sapiens | Heart Disease,Childhood Acute Lymphocytic Leukemia,Childhood T-Cell Acute Lymphoblastic Leukemia,Myeloid And Lymphoid Neoplasms Associated With Pdgfra Rearrangement,Chronic Neutrophilic Leukemia,Melanoma,Chronic Eosinophilic Leukemia,Leukemia, Chronic Myeloid,B-Lymphoblastic Leukemia/Lymphoma,B-Lymphoblastic Leukemia/Lymphoma With Bcr-Abl1,B-Lymphoblastic Leukemia/Lymphoma With Hypodiploidy,B-Lymphoblastic Leukemia/Lymphoma, Bcr-Abl1-Like,B-Lymphoblastic Leukemia/Lymphoma With Iamp21,Lung Large Cell Carcinoma,Blood Platelet Disease,Essential Thrombocythemia,Myeloproliferative Neoplasm,Testicular Leukemia,Philadelphia-Negative Chronic Myeloid Leukemia,Leukemia,Mixed Phenotype Acute Leukemia,Myelophthisic Anemia,Blood Coagulation Disease,Hypereosinophilic Syndrome,Childhood Leukemia,Leukemia, Acute Myeloid,Bone Marrow Cancer,Myelodysplastic/Myeloproliferative Neoplasm,Hematologic Cancer,Leukemia, Acute Lymphoblastic,Moyamoya Angiopathy,Polycythemia,Leiomyomatosis,Central Nervous System Leukemia,Precursor T-Cell Acute Lymphoblastic Leukemia,Acquired Polycythemia,T-Cell Prolymphocytic Leukemia,Chronic Leukemia,Cockayne Syndrome,Prolymphocytic Leukemia,Lip And Oral Cavity Cancer,Ovarian Cancer,Myeloid Leukemia,T-Cell Acute Lymphoblastic Leukemia,Adult Acute Lymphocytic Leukemia,Breast Cancer,Colorectal Cancer,Congenital Heart Defects And Skeletal Malformations Syndrome,Deficiency Anemia,Leukemia, Acute Lymphoblastic 3,Retinoblastoma,Mental Retardation, Autosomal Dominant 29,Myelodysplastic Syndrome,Mental Retardation, Autosomal Dominant 33,Gastrointestinal Stromal Tumor,Lymphoblastic Leukemia, Acute, With Lymphomatous Features,Wilms Tumor 1,Leukemia, Chronic Lymphocytic,Dermatofibrosarcoma Protuberans,Ataxia-Telangiectasia,B-Cell Adult Acute Lymphocytic Leukemia,Atypical Chronic Myeloid Leukemia,Polycythemia Vera |
2f4j_a | P00519 | ENSG00000097007 | ABL1 | 98.90 | 9.40E-14 | 1.10E-17 | 125.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | RAD53 MEC2 SAD1 SPK1 YPL153C P2588 |
Serine/threonine-protein kinase RAD53 (EC 2.7.12.1) (CHEK2 homolog) (Serine-protein kinase 1) |
2.7.12.1 | Saccharomyces cerevisiae | 4pdp_a | P22216 | 98.90 | 3.20E-13 | 3.70E-17 | 127.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YNL154C | YCK2 | SGDID:S000005098 | CSNK1G2 CK1G2 |
Casein kinase I isoform gamma-2 (CKI-gamma 2) (EC 2.7.11.1) |
2.7.11.1 | Homo sapiens | Familial Febrile Seizures |
2c47_d | P78368 | ENSG00000133275 | CSNK1G2 | 99.70 | 1.90E-22 | 2.10E-26 | 192.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | NTRK2 TRKB |
BDNF/NT-3 growth factors receptor (EC 2.7.10.1) (GP145-TrkB) (Trk-B) (Neurotrophic tyrosine kinase receptor type 2) (TrkB tyrosine kinase) (Tropomyosin-related kinase B) |
2.7.10.1 | Homo sapiens | Ganglioneuroblastoma,Kagami-Ogata Syndrome,Status Epilepticus,Peripheral Nervous System Benign Neoplasm,Autonomic Nervous System Benign Neoplasm,Peripheral Nervous System Neoplasm,Alcohol Dependence,Alzheimer Disease,Major Depressive Disorder,Amyotrophic Lateral Sclerosis 1,Undetermined Early-Onset Epileptic Encephalopathy,Paranoid Schizophrenia,Leptin Deficiency Or Dysfunction,Congenital Mesoblastic Nephroma,Ganglioneuroma,Neuroblastoma,Pilomyxoid Astrocytoma,Pilocytic Astrocytoma,Ganglioglioma,Congenital Fibrosarcoma,Autonomic Nervous System Neoplasm,Obsessive-Compulsive Disorder,Sudden Infant Death Syndrome,Nodular Ganglioneuroblastoma,Malignant Giant Cell Tumor Of The Tendon Sheath,Adenocarcinoma,Neuropathy, Hereditary Sensory And Autonomic, Type Iii,Breast Cancer,Parkinson Disease, Late-Onset,Peripheral Nervous System Disease,Oligodendroglioma,Bipolar Disorder,Temporal Lobe Epilepsy,Developmental And Epileptic Encephalopathy 58,West Syndrome,Disease Of Mental Health,Pediatric Fibrosarcoma,Toxic Encephalopathy,Body Mass Index Quantitative Trait Locus 11,Mental Depression,Olfactory Neuroblastoma,Multiple Sclerosis,Obesity, Hyperphagia, And Developmental Delay,Fragile X Syndrome,Schizophrenia,Asperger Syndrome,Hereditary Sensory Neuropathy,Large Cell Neuroendocrine Carcinoma,Attention Deficit-Hyperactivity Disorder,Wilms Tumor 1,Wilms Tumor, Aniridia, Genitourinary Anomalies, And Mental Retardation Syndrome,Anxiety,Medulloblastoma,Autism,Central Hypoventilation Syndrome, Congenital,Christianson Syndrome |
4asz_a | Q16620 | ENSG00000148053 | NTRK2 | 99.00 | 2.20E-14 | 2.60E-18 | 130.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | ROP5B ROP5 TGRH88_057710 |
ROP5B ROP5 TGRH88_057710 |
Toxoplasma gondii | 4lv5_a | F2YGR7 | 98.90 | 3.10E-13 | 3.50E-17 | 129.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YNL154C | YCK2 | SGDID:S000005098 | IGF1R |
Insulin-like growth factor 1 receptor (EC 2.7.10.1) (Insulin-like growth factor I receptor) (IGF-I receptor) (CD antigen CD221) [Cleaved into: Insulin-like growth factor 1 receptor alpha chain; Insulin-like growth factor 1 receptor beta chain] |
2.7.10.1 | Homo sapiens | Pancreatic Adenocarcinoma,Bone Disease,Skin Melanoma,Acanthosis Nigricans,Neuroendocrine Tumor,Endometrial Cancer,Autosomal Dominant Polycystic Kidney Disease,Squamous Cell Carcinoma,Hyperglycemia,Lung Cancer Susceptibility 3,Chromosome 15q26-Qter Deletion Syndrome,Rhabdomyosarcoma 2,Polycystic Kidney Disease,Vagina Sarcoma,Melanoma,Thyroid Gland Anaplastic Carcinoma,Diabetes Mellitus,Dedifferentiated Liposarcoma,Hyperinsulinism,Clear Cell Renal Cell Carcinoma,Odontogenic Myxoma,Atypical Teratoid Rhabdoid Tumor,Amelogenesis Imperfecta,Short Syndrome,Graves' Disease,Insulin-Like Growth Factor I,Craniosynostosis,Neuroblastoma,Ring Chromosome 15,Vaginal Endometrial Stromal Sarcoma,Hyperinsulinemic Hypoglycemia,Ring Chromosome,Osteoporosis,Nk-Cell Enteropathy,Ovarian Cancer,Adenocarcinoma,Breast Cancer,Glioblastoma,Colorectal Cancer,Hepatocellular Carcinoma,Malignant Peripheral Nerve Sheath Tumor,Rhabdomyosarcoma,Prostate Embryonal Rhabdomyosarcoma,Myxoid Liposarcoma,Ovarian Disease,Localized Osteosarcoma,Liposarcoma,Skin Carcinoma,Gastric Cancer,Prostate Cancer,Disease Of Mental Health,Rhabdoid Cancer,Adrenal Cortical Carcinoma,Type 2 Diabetes Mellitus,Silver-Russell Syndrome 1,Lung Squamous Cell Carcinoma,Adrenal Cortex Disease,Skeletal Muscle Cancer,Muscle Cancer,Beckwith-Wiedemann Syndrome,Sarcoma, Synovial,Esophageal Cancer,Askin'S Tumor,Hypotrichosis 10,Ewing Sarcoma,Lymphangioleiomyomatosis,Donohue Syndrome,Paraganglioma And Gastric Stromal Sarcoma,Renal Cell Carcinoma, Nonpapillary,Wilms Tumor 1,Nijmegen Breakage Syndrome,Amelogenesis Imperfecta, Type Ig,Medulloblastoma,Melanoma, Uveal,Lung Cancer,Osteogenic Sarcoma,Pancreatic Cancer,Polycythemia Vera |
1p4o_b | P08069 | ENSG00000140443 | IGF1R | 98.90 | 9.90E-14 | 1.20E-17 | 128.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | EPHA3 ETK ETK1 HEK TYRO4 |
Ephrin type-A receptor 3 (EC 2.7.10.1) (EPH-like kinase 4) (EK4) (hEK4) (HEK) (Human embryo kinase) (Tyrosine-protein kinase TYRO4) (Tyrosine-protein kinase receptor ETK1) (Eph-like tyrosine kinase 1) |
2.7.10.1 | Homo sapiens | Large Cell Carcinoma,Lung Large Cell Carcinoma,Cerebral Artery Occlusion,Adenocarcinoma,Breast Cancer,Beriberi,Parkinson Disease, Late-Onset,Colorectal Cancer,Thiamine Deficiency Disease,Tumoral Calcinosis, Hyperphosphatemic, Familial, 1,Wet Beriberi |
2qoc_a | P29320 | ENSG00000044524 | EPHA3 | 99.00 | 5.20E-14 | 6.10E-18 | 132.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | DMPK DM1PK MDPK |
Myotonin-protein kinase (MT-PK) (EC 2.7.11.1) (DM-kinase) (DMK) (DM1 protein kinase) (DMPK) (Myotonic dystrophy protein kinase) |
2.7.11.1 | Homo sapiens | Muscular Disease,Fuchs' Endothelial Dystrophy,Myopathy,Muscle Tissue Disease,Neuromuscular Disease,Hypertrophic Cardiomyopathy,Myotonic Disease,Myotonic Dystrophy 1,Muscular Dystrophy,Myotonic Dystrophy,Spinocerebellar Ataxia 8,Myotonic Cataract,Cataract,Oculopharyngeal Muscular Dystrophy,Hair Follicle Neoplasm,Myotonic Dystrophy 2,Myotonia,Immature Cataract,Lens Disease,Autosomal Dominant Cerebellar Ataxia,Disease Of Mental Health,Fragile X Syndrome,Huntington Disease-Like 2,First-Degree Atrioventricular Block,Fragile X-Associated Tremor/Ataxia Syndrome,X-Linked Hereditary Ataxia,Spinal And Bulbar Muscular Atrophy, X-Linked 1,Catecholaminergic Polymorphic Ventricular Tachycardia,Frontotemporal Dementia,3-Methylglutaconic Aciduria, Type Iii |
2vd5_a | Q09013 | ENSG00000104936 | DMPK | 98.90 | 2.00E-13 | 2.30E-17 | 132.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | CPK4 CDPK4 PF07_0072 |
Calcium-dependent protein kinase 4 (EC 2.7.11.1) |
2.7.11.1 | Plasmodium falciparum | 4rgj_a | Q8IBS5 | 98.80 | 3.40E-13 | 4.10E-17 | 132.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YNL154C | YCK2 | SGDID:S000005098 | VRK1 |
Serine/threonine-protein kinase VRK1 (EC 2.7.11.1) (Vaccinia-related kinase 1) |
2.7.11.1 | Homo sapiens | Congenital Contractures,Axonal Neuropathy,Spinal Muscular Atrophy,Microcephaly-Complex Motor And Sensory Axonal Neuropathy Syndrome,Pontocerebellar Hypoplasia Type 1,Muscular Atrophy,Anterior Horn Cell Disease,Polyhydramnios,Juvenile Amyotrophic Lateral Sclerosis,Neuropathy,Microcephaly,Epidermolysis Bullosa, Junctional, Herlitz Type,Vaccinia,Pontocerebellar Hypoplasia, Type 5,Pontocerebellar Hypoplasia, Type 9,Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia,Pontocerebellar Hypoplasia, Type 1b,Pontocerebellar Hypoplasia, Type 1a,Pontocerebellar Hypoplasia,Autosomal Recessive Non-Syndromic Intellectual Disability,Peho Syndrome |
2rsv_a | Q99986 | ENSG00000100749 | VRK1 | 99.20 | 2.50E-15 | 2.80E-19 | 146.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | OXSR1 KIAA1101 OSR1 |
Serine/threonine-protein kinase OSR1 (EC 2.7.11.1) (Oxidative stress-responsive 1 protein) |
2.7.11.1 | Homo sapiens | Bartter Disease,Arthrogryposis, Distal, Type 3,Hypomagnesemia 4, Renal,Distal Arthrogryposis,Hypomagnesemia 3, Renal |
3dak_d | O95747 | ENSG00000172939 | OXSR1 | 98.90 | 1.60E-13 | 1.90E-17 | 123.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | FGFR2 BEK KGFR KSAM |
Fibroblast growth factor receptor 2 (FGFR-2) (EC 2.7.10.1) (K-sam) (KGFR) (Keratinocyte growth factor receptor) (CD antigen CD332) |
2.7.10.1 | Homo sapiens | Bone Disease,Acanthosis Nigricans,Bone Development Disease,Achondroplasia,Physical Disorder,Uterine Carcinosarcoma,Endometrial Cancer,Apert Syndrome,Clear Cell Acanthoma,Autosomal Dominant Polycystic Kidney Disease,Saethre-Chotzen Syndrome,Acanthoma,Squamous Cell Carcinoma,Pfeiffer Syndrome,Lung Cancer Susceptibility 3,Calcinosis,Polycystic Kidney Disease,Pleuropulmonary Blastoma,Acne,Dysostosis,Exophthalmos,Familial Scaphocephaly Syndrome,Exposure Keratitis,Synostosis,Dysgerminoma,Skin Tag,Rasopathy,Deafness, Autosomal Recessive 71,Ectodermal Dysplasia,Brachyolmia Type 4 With Mild Epiphyseal And Metaphyseal Changes,Holoprosencephaly,Split Hand-Foot Malformation,Ankylosis,Cervical Keratinizing Squamous Cell Carcinoma,Radioulnar Synostosis,Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate,Plagiocephaly,Syndromic Craniosynostosis,Craniosynostosis,Chronic Inflammation Of Lacrimal Passage,Dacryocystocele,Bile Duct Adenocarcinoma,Esophagus Adenocarcinoma,Nevus, Epidermal,Luteoma,Testicular Spermatocytic Seminoma,Intrahepatic Cholangiocarcinoma,Glioma,Fibrolamellar Carcinoma,Hepatocellular Clear Cell Carcinoma,Cytochrome P450 Oxidoreductase Deficiency,Fgfr Craniosynostosis Syndromes,Bladder Cancer,Pigmentation Disease,Wolffian Duct Adenocarcinoma,Osteoglophonic Dysplasia,Endometrial Adenocarcinoma,Adult Teratoma,Ovarian Cancer,Adenocarcinoma,Eccrine Papillary Adenocarcinoma,Breast Cancer,Glioblastoma,Wells Syndrome,Colorectal Cancer,Hypospadias,Hydrocephalus,Cholesteatoma Of Middle Ear,Scaphocephaly, Maxillary Retrusion, And Mental Retardation,Muenke Syndrome,Syringomyelia,Myxoid Liposarcoma,Van Der Woude Syndrome 1,Cleft Palate, Isolated,Cleidocranial Dysplasia,Gastric Cancer,Prostate Cancer,Disease Of Mental Health,Cholangiocarcinoma,Craniosynostosis 1,Jackson-Weiss Syndrome,Kallmann Syndrome,Crouzon Syndrome,Beare-Stevenson Cutis Gyrata Syndrome,Skin Disease,Gastric Adenocarcinoma,Porokeratosis,Aplasia Of Lacrimal And Salivary Glands,Lung Squamous Cell Carcinoma,Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1,Hydrocephalus, Congenital, 1,Antley-Bixler Syndrome,Split-Hand/Foot Malformation 1,Esophageal Cancer,Hypertelorism, Microtia, Facial Clefting Syndrome,Odontochondrodysplasia,Orofacial Cleft,Strabismus,Hemifacial Hyperplasia,Chromosome 2q35 Duplication Syndrome,Tooth Agenesis,Thanatophoric Dysplasia, Type I,Renal Hypodysplasia/Aplasia 1,Humeroradial Synostosis,Vesicoureteral Reflux 1,Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans,Nasopharyngeal Carcinoma,Bent Bone Dysplasia Syndrome,Hypertelorism,Hypochondroplasia,Estrogen-Receptor Positive Breast Cancer,Carpenter Syndrome 1,Lacrimoauriculodentodigital Syndrome,Scoliosis,Antley-Bixler Syndrome Without Genital Anomalies Or Disordered Steroidogenesis,Chromosomal Duplication Syndrome,Lung Cancer,Pancreatic Cancer,Peters-Plus Syndrome,Multiple Pterygium Syndrome, Escobar Variant |
2psq_a | P21802 | ENSG00000066468 | FGFR2 | 99.20 | 3.00E-15 | 3.50E-19 | 142.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | EPHA5 BSK EHK1 HEK7 TYRO4 |
Ephrin type-A receptor 5 (EC 2.7.10.1) (Brain-specific kinase) (EPH homology kinase 1) (EHK-1) (EPH-like kinase 7) (EK7) (hEK7) |
2.7.10.1 | Homo sapiens | Lung Cancer Susceptibility 3,Large Cell Carcinoma,Lung Large Cell Carcinoma,Adenocarcinoma,Leber Congenital Amaurosis 17,Polyneuropathy Due To Drug,Lung Cancer |
2r2p_a | P54756 | ENSG00000145242 | EPHA5 | 98.90 | 3.10E-13 | 3.70E-17 | 123.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | RPS6KA1 MAPKAPK1A RSK1 |
Ribosomal protein S6 kinase alpha-1 (S6K-alpha-1) (EC 2.7.11.1) (90 kDa ribosomal protein S6 kinase 1) (p90-RSK 1) (p90RSK1) (p90S6K) (MAP kinase-activated protein kinase 1a) (MAPK-activated protein kinase 1a) (MAPKAP kinase 1a) (MAPKAPK-1a) (Ribosomal S6 kinase 1) (RSK-1) |
2.7.11.1 | Homo sapiens | Tuberous Sclerosis 2,Tuberous Sclerosis,Cardiomyopathy, Familial Hypertrophic, 4,Disease Of Mental Health,Adrenal Cortical Adenocarcinoma,Dyskeratosis Congenita, Autosomal Dominant 3,Tuberous Sclerosis 1,Coffin-Lowry Syndrome,Polycystic Kidney Disease 3 With Or Without Polycystic Liver Disease |
4nif_d | Q15418 | ENSG00000117676 | RPS6KA1 | 99.10 | 1.60E-14 | 1.80E-18 | 136.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | CDC42BPB KIAA1124 |
Serine/threonine-protein kinase MRCK beta (EC 2.7.11.1) (CDC42-binding protein kinase beta) (CDC42BP-beta) (DMPK-like beta) (Myotonic dystrophy kinase-related CDC42-binding kinase beta) (MRCK beta) (Myotonic dystrophy protein kinase-like beta) |
2.7.11.1 | Homo sapiens | Myotonic Dystrophy,Epidermolysis Bullosa Simplex, Dowling-Meara Type |
5ote_a | Q9Y5S2 | ENSG00000198752 | CDC42BPB | 98.90 | 1.20E-13 | 1.40E-17 | 134.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | Camk1 |
Calcium/calmodulin-dependent protein kinase type 1 (EC 2.7.11.17) (CaM kinase I) (CaM-KI) (CaM kinase I alpha) (CaMKI-alpha) |
2.7.11.17 | Rattus norvegicus | 1a06_a | Q63450 | 99.40 | 9.90E-18 | 1.00E-21 | 164.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YNL154C | YCK2 | SGDID:S000005098 | FES FPS |
Tyrosine-protein kinase Fes/Fps (EC 2.7.10.2) (Feline sarcoma/Fujinami avian sarcoma oncogene homolog) (Proto-oncogene c-Fes) (Proto-oncogene c-Fps) (p93c-fes) |
2.7.10.2 | Homo sapiens | Melanoma,Leukemia, Chronic Myeloid,Latent Syphilis,Sjogren-Larsson Syndrome,Leukemia,Myeloid Leukemia,Sarcoma,Ewing Sarcoma Of Bone,Neurofibrosarcoma,Acute Promyelocytic Leukemia,Miller-Dieker Lissencephaly Syndrome,Myopathy, Centronuclear, 2 |
3cbl_a | P07332 | ENSG00000182511 | FES | 99.00 | 1.80E-14 | 2.10E-18 | 136.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | HRR25 YPL204W |
Casein kinase I homolog HRR25 (EC 2.7.11.1) |
2.7.11.1 | Saccharomyces cerevisiae | 5cyz_a | P29295 | 99.50 | 3.90E-18 | 4.50E-22 | 165.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YNL154C | YCK2 | SGDID:S000005098 | TNK2 ACK1 |
Activated CDC42 kinase 1 (ACK-1) (EC 2.7.10.2) (EC 2.7.11.1) (Tyrosine kinase non-receptor protein 2) |
2.7.10.2 | Homo sapiens | Gastric Cardia Carcinoma,Epilepsy,Infantile-Onset Mesial Temporal Lobe Epilepsy With Severe Cognitive Regression,Parkinson Disease, Late-Onset |
4ewh_a | Q07912 | ENSG00000061938 | TNK2 | 99.00 | 2.00E-14 | 2.50E-18 | 127.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | gish anon-WO0118547.425 CK1 CK1-gamma CK1[[gamma]] CK1gamma CKI-related CKIgamma Dmel\CG6963 Gish Hrr25 ms(3)89B NEST:bs27c08 Spider spider CG6963 Dmel_CG6963 |
gish anon-WO0118547.425 CK1 CK1-gamma CK1[[gamma]] CK1gamma CKI-related CKIgamma Dmel\CG6963 Gish Hrr25 ms(3)89B NEST:bs27c08 Spider spider CG6963 Dmel_CG6963 |
2.7.11.- | Drosophila melanogaster | 4nt4_a | Q86NK8 | 99.40 | 1.70E-17 | 2.10E-21 | 150.60 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | |||
YNL154C | YCK2 | SGDID:S000005098 | JAK2 |
Tyrosine-protein kinase JAK2 (EC 2.7.10.2) (Janus kinase 2) (JAK-2) |
2.7.10.2 | Homo sapiens | Myeloid And Lymphoid Neoplasms Associated With Pdgfra Rearrangement,Chronic Neutrophilic Leukemia,Chronic Myelomonocytic Leukemia,Portal Vein Thrombosis,Polycystic Kidney Disease,Chronic Eosinophilic Leukemia,Leukemia, Chronic Myeloid,Gaucher'S Disease,B-Lymphoblastic Leukemia/Lymphoma, Bcr-Abl1-Like,B-Cell Lymphoma,Acute Erythroid Leukemia,Core Binding Factor Acute Myeloid Leukemia,Hemorrhagic Disease,Blood Platelet Disease,Essential Thrombocythemia,Myeloproliferative Neoplasm,Thrombocytosis,Leptin Deficiency Or Dysfunction,Sm-Ahnmd,Leukemia,Myelophthisic Anemia,Blood Coagulation Disease,Hypereosinophilic Syndrome,Wernicke Encephalopathy,Acquired Von Willebrand Syndrome,Neutrophilia, Hereditary,Acute Leukemia,Central Retinal Vein Occlusion,Thrombophilia,Leukemia, Acute Myeloid,Primary Mediastinal Large B-Cell Lymphoma,Refractory Anemia,Bone Marrow Cancer,Myelodysplastic/Myeloproliferative Neoplasm,Hematologic Cancer,Splenic Infarction,Leukemia, Acute Lymphoblastic,Cebpa-Associated Familial Acute Myeloid Leukemia,Polycythemia,Dilated Cardiomyopathy,Etv6 Thrombocytopenia And Predisposition To Leukemia,Behcet Syndrome,Hepatic Vascular Disease,Antithrombin Iii Deficiency,Splenomegaly,Acquired Polycythemia,Chronic Leukemia,Diamond-Blackfan Anemia,Mixed Lacrimal Gland Cancer,Erythrocytosis, Familial, 8,Vein Disease,Ovarian Cancer,Myeloid Leukemia,Acute Megakaryocytic Leukemia,Crohn'S Disease,Breast Cancer,Colorectal Cancer,Portal Hypertension,Primary Polycythemia,Premature Menopause,Combined Oxidative Phosphorylation Deficiency 16,Benign Essential Hypertension,Deficiency Anemia,Sarcoma,Fibrosarcoma,Systemic Mastocytosis,Prostate Cancer,Disease Of Mental Health,Mastocytosis,Sagittal Sinus Thrombosis,Body Mass Index Quantitative Trait Locus 11,Thrombocytopenia,Renovascular Hypertension,Amegakaryocytic Thrombocytopenia, Congenital,Beta-Thalassemia,Lymphoma, Non-Hodgkin, Familial,Mouth Disease,Lymphoma, Hodgkin, Classic,Erythrocytosis, Familial, 1,Inflammatory Bowel Disease,Severe Congenital Neutropenia,Myelodysplastic Syndrome,Mental Retardation, Autosomal Dominant 33,Down Syndrome,Gastrointestinal Stromal Tumor,Lymphoblastic Leukemia, Acute, With Lymphomatous Features,Thrombocythemia 3,Hypertension, Essential,Ischemic Colitis,Leukemia, Chronic Lymphocytic,Juvenile Myelomonocytic Leukemia,Systemic Lupus Erythematosus,Premature Ovarian Failure 1,Myelofibrosis,Myeloma, Multiple,Medulloblastoma,Atypical Chronic Myeloid Leukemia,Thrombosis,Lung Cancer,Asthma,Budd-Chiari Syndrome,Polycythemia Vera |
3krr_a | O60674 | ENSG00000096968 | JAK2 | 98.90 | 2.20E-13 | 2.70E-17 | 122.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | BRAF BRAF1 RAFB1 |
Serine/threonine-protein kinase B-raf (EC 2.7.11.1) (Proto-oncogene B-Raf) (p94) (v-Raf murine sarcoma viral oncogene homolog B1) |
2.7.11.1 | Homo sapiens | Spitzoid Melanoma,Melanoma In Congenital Melanocytic Nevus,Ventricular Septal Defect,Pancreatic Adenocarcinoma,Melanotic Neuroectodermal Tumor,Skin Melanoma,Gliomatosis Cerebri,Endometrial Cancer,Autosomal Dominant Polycystic Kidney Disease,Endosalpingiosis,Follicular Adenoma,Squamous Cell Carcinoma,Brain Stem Glioma,Thyroid Gland Cancer,Lung Cancer Susceptibility 3,Acral Lentiginous Melanoma,Metanephric Adenoma,Pulmonary Valve Stenosis,Primary Mediastinal B-Cell Lymphoma,Polycystic Kidney Disease,Suppression Of Tumorigenicity 12,Melanoma,Leukemia, Chronic Myeloid,Plasma Cell Neoplasm,Erdheim-Chester Disease,Thyroid Gland Anaplastic Carcinoma,Posterior Uveal Melanoma,Adenoma,Amelanotic Melanoma,Granulomatous Dermatitis,Acneiform Dermatitis,Juvenile Xanthogranuloma,Hypertrophic Cardiomyopathy,Childhood Pilocytic Astrocytoma,Rasopathy,Nonseminomatous Germ Cell Tumor,Desmoplastic Infantile Astrocytoma,Desmoplastic Infantile Ganglioglioma,Tall Cell Variant Papillary Carcinoma,Refractory Hairy Cell Leukemia,Refractory Hematologic Cancer,Costello Syndrome,Astroblastoma,Differentiated Thyroid Carcinoma,Eosinophilic Cystitis,Familial Colorectal Cancer,Leukemia,Colon Adenocarcinoma,Colonic Benign Neoplasm,Pilomyxoid Astrocytoma,Cerebellar Astrocytoma,Pilocytic Astrocytoma,Pleomorphic Xanthoastrocytoma,Pilocytic Astrocytoma Of Cerebellum,Diffuse Astrocytoma,Serrated Polyposis Syndrome,Pseudo-Turner Syndrome,Arteriovenous Malformations Of The Brain,Wilms Tumor 5,Glioma,Noonan Syndrome 1,Newborn Respiratory Distress Syndrome,Respiratory Distress Syndrome, Infant,Rhabdoid Meningioma,Noonan Syndrome And Noonan-Related Syndrome,Ganglioglioma,Neuronal Tumor,Desmoplastic Infantile Astrocytoma/Ganglioglioma,Papillary Tumor Of The Pineal Region,Dandy-Walker Syndrome,Struma Ovarii,Transitional Cell Carcinoma,Rosai-Dorfman Disease,Classic Hairy Cell Leukemia,Adenofibroma,Benign Struma Ovarii,Thyroid Carcinoma,Nodular Malignant Melanoma,Bladder Cancer,Thyroid Tumor,Brain Cancer,Spitz Nevus,Nodular Goiter,Testicular Germ Cell Tumor,Hairy Cell Leukemia,Lip Cancer,Syringocystadenoma Papilliferum,Lip And Oral Cavity Cancer,Mature Teratoma,Ovarian Cancer,Nevus Of Ota,Adenocarcinoma,Myopericytoma,Urachal Adenocarcinoma,Breast Cancer,Glioblastoma,Squamous Cell Carcinoma, Head And Neck,Malignant Astrocytoma,High Grade Glioma,Gliosarcoma,Giant Cell Glioblastoma,Juvenile Astrocytoma,Colorectal Cancer,Ovarian Serous Cystadenocarcinoma,Cystadenocarcinoma,Papillary Carcinoma,Serous Cystadenocarcinoma,Hepatocellular Carcinoma,Skin Squamous Cell Carcinoma,Skin Benign Neoplasm,Verrucous Papilloma,Cardiofaciocutaneous Syndrome 1,Tethered Spinal Cord Syndrome,Cardiomyopathy, Familial Hypertrophic, 4,Noonan Syndrome With Multiple Lentigines,Sarcoma,Hypothyroidism,Histiocytosis,Skin Carcinoma,Gastric Cancer,Prostate Cancer,Papillary Thyroid Microcarcinoma,Cholangiocarcinoma,Noonan Syndrome 7,Leopard Syndrome 3,Panniculitis,Adrenal Cortical Carcinoma,Ovary Adenocarcinoma,Gastric Adenocarcinoma,Nephrotic Syndrome, Type 3,Craniopharyngioma,Melphalan Allergy,Papillary Craniopharyngioma,Lynch Syndrome,Apocrine Adenoma,Lung Squamous Cell Carcinoma,Adrenal Carcinoma,Thyroid Gland Follicular Carcinoma,Langerhans Cell Histiocytosis,Thyroid Gland Papillary Carcinoma,Bladder Urothelial Carcinoma,Lymphoma, Non-Hodgkin, Familial,Renal Cell Carcinoma, Papillary, 1,Thyroid Cancer, Nonmedullary, 2,Thyroid Cancer, Nonmedullary, 1,Phace Association,Colorectal Cancer, Hereditary Nonpolyposis, Type 5,Hashimoto Thyroiditis,Gastrointestinal Stromal Tumor,Colorectal Adenocarcinoma,Villous Adenoma,Renal Cell Carcinoma, Nonpapillary,Mucosal Melanoma,Wilms Tumor 1,Hypertelorism,Lymphoma,Colitis,Lentigines,Leopard Syndrome 1,Leukemia, Chronic Lymphocytic,Juvenile Myelomonocytic Leukemia,Myeloma, Multiple,Melanoma, Cutaneous Malignant 1,Melanoma, Uveal,Lung Cancer,Pancreatic Cancer,Multiple Pterygium Syndrome, Escobar Variant,Pulmonic Stenosis |
4h58_c | P15056 | ENSG00000157764 | BRAF | 99.10 | 4.30E-15 | 5.20E-19 | 132.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | JAK3 |
Tyrosine-protein kinase JAK3 (EC 2.7.10.2) (Janus kinase 3) (JAK-3) (Leukocyte janus kinase) (L-JAK) |
2.7.10.2 | Homo sapiens | Lymphopenia,Reticular Dysgenesis,Severe Combined Immunodeficiency,Myeloproliferative Syndrome, Transient,Common Variable Immunodeficiency,Myeloproliferative Neoplasm,Leukemia,Childhood Leukemia,Leukemia, Acute Myeloid,Leukemia, Acute Lymphoblastic,Combined Immunodeficiency,Autoimmune Disease,T-B- Severe Combined Immunodeficiency,Geotrichosis,Sezary'S Disease,T-Cell Prolymphocytic Leukemia,Prolymphocytic Leukemia,Nk-Cell Enteropathy,T-Cell Adult Acute Lymphocytic Leukemia,T-Cell Acute Lymphoblastic Leukemia,Acute Megakaryocytic Leukemia,Adenosine Deaminase Deficiency,Jak3-Deficient Severe Combined Immunodeficiency,Alk-Positive Anaplastic Large Cell Lymphoma,Hyper Ige Recurrent Infection Syndrome 1,Chronic Granulomatous Disease,Omenn Syndrome,Severe Combined Immunodeficiency, X-Linked,Adult T-Cell Leukemia,Immunodeficiency 35,Immune Deficiency Disease,Immunodeficiency 63 With Lymphoproliferation And Autoimmunity,Mature T-Cell And Nk-Cell Lymphoma,Anaplastic Large Cell Lymphoma,Peripheral T-Cell Lymphoma,Down Syndrome,Lymphoblastic Leukemia, Acute, With Lymphomatous Features,Bone Squamous Cell Carcinoma,Janus Kinase-3 Deficiency,Cd40 Ligand Deficiency,Jacobsen Syndrome,Alopecia Universalis Congenita,Juvenile Myelomonocytic Leukemia,Myelofibrosis,Bare Lymphocyte Syndrome, Type Ii,Lung Cancer,Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Negative,Polycythemia Vera |
1yvj_a | P52333 | ENSG00000105639 | JAK3 | 98.90 | 1.50E-13 | 1.90E-17 | 123.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | PTK6 BRK |
Protein-tyrosine kinase 6 (EC 2.7.10.2) (Breast tumor kinase) (Tyrosine-protein kinase BRK) |
2.7.10.2 | Homo sapiens | Charge Syndrome,Aggressive Systemic Mastocytosis,Breast Cancer,Inclusion Conjunctivitis,Ovary Serous Adenocarcinoma,Thoracic Outlet Syndrome |
6cz4_a | Q13882 | ENSG00000101213 | PTK6 | 98.90 | 2.60E-13 | 3.20E-17 | 119.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | DYRK2 |
Dual specificity tyrosine-phosphorylation-regulated kinase 2 (EC 2.7.12.1) |
2.7.12.1 | Homo sapiens | 4azf_a | Q92630 | ENSG00000127334 | DYRK2 | 99.00 | 6.30E-14 | 7.00E-18 | 137.80 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YNL154C | YCK2 | SGDID:S000005098 | MARK1 KIAA1477 MARK |
Serine/threonine-protein kinase MARK1 (EC 2.7.11.1) (EC 2.7.11.26) (MAP/microtubule affinity-regulating kinase 1) (PAR1 homolog c) (Par-1c) (Par1c) |
2.7.11.26 | Homo sapiens | Alzheimer Disease,Peutz-Jeghers Syndrome,Autism |
6c9d_a | Q9P0L2 | ENSG00000116141 | MARK1 | 98.90 | 2.10E-13 | 2.20E-17 | 137.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | EGFR ERBB ERBB1 HER1 |
Epidermal growth factor receptor (EC 2.7.10.1) (Proto-oncogene c-ErbB-1) (Receptor tyrosine-protein kinase erbB-1) |
2.7.10.1 | Homo sapiens | Esophageal Disease,Benign Breast Adenomyoepithelioma,Pancreatic Adenocarcinoma,Supratentorial Cancer,Skin Melanoma,Gliomatosis Cerebri,Uterine Body Mixed Cancer,Nail Disease,Uterine Carcinosarcoma,Endometrial Cancer,Epithelioid Sarcoma,Autosomal Dominant Polycystic Kidney Disease,Spinal Chordoma,Peritoneum Cancer,Allergic Cutaneous Vasculitis,Squamous Cell Carcinoma,Inflammatory Breast Carcinoma,Retinitis Pigmentosa,Brain Stem Glioma,Thyroid Gland Cancer,Hair Disease,Peritoneal Mesothelioma,Lung Cancer Susceptibility 3,Sebaceous Gland Disease,Penile Cancer,Adenoid Cystic Carcinoma,Carcinosarcoma,Submandibular Gland Cancer,Chordoma,Bone Cancer,Cowden Syndrome,Signet Ring Lung Adenocarcinoma,Polycystic Kidney Disease,Hepatitis C,Suppression Of Tumorigenicity 12,Melanoma,Leukemia, Chronic Myeloid,Gastroesophageal Adenocarcinoma,Lung Non-Squamous Non-Small Cell Carcinoma,Thyroid Gland Anaplastic Carcinoma,Diabetes Mellitus,Cowden Syndrome 1,Primary Peritoneal Carcinoma,Malignant Peritoneal Mesothelioma,Papillary Squamous Carcinoma,Cholecystitis,Acneiform Dermatitis,Covid-19,Rectum Adenocarcinoma,Synchronous Bilateral Breast Carcinoma,Peripheral Nervous System Neoplasm,Uterine Corpus Cancer,Connective Tissue Cancer,Drug-Induced Hepatitis,Frontal Lobe Neoplasm,Clear Cell Renal Cell Carcinoma,Vulvar Disease,Rasopathy,Vulva Squamous Cell Carcinoma,Acth-Secreting Pituitary Adenoma,Mucoepidermoid Carcinoma,Large Cell Carcinoma,Keratosis Pilaris Atrophicans Faciei,Neurofibroma,Esophageal Basaloid Squamous Cell Carcinoma,Bile Duct Cancer,Intestinal Benign Neoplasm,Malignant Ovarian Surface Epithelial-Stromal Neoplasm,Ovary Epithelial Cancer,Oral Cancer,Orbital Lymphangioma,Doxorubicin Induced Cardiomyopathy,Mammary Analogue Secretory Carcinoma,Amelogenesis Imperfecta,Human Cytomegalovirus Infection,Retinal Cancer,Biliary Tract Disease,Breast Metaplastic Carcinoma,Myeloproliferative Neoplasm,Differentiated Thyroid Carcinoma,Glial Tumor,Hepatitis,Infratentorial Cancer,Malignant Pleural Mesothelioma,Pulmonary Blastoma,Neurofibromatosis, Type I,Breast Scirrhous Carcinoma,Asbestos-Related Lung Carcinoma,Colon Adenocarcinoma,Adenosquamous Lung Carcinoma,Vulva Cancer,Adenosquamous Carcinoma,Neuroblastoma,Colonic Benign Neoplasm,Diffuse Astrocytoma,Bile Duct Adenocarcinoma,Esophagus Adenocarcinoma,Arteriovenous Malformations Of The Brain,Inherited Cancer-Predisposing Syndrome,Bronchiolo-Alveolar Adenocarcinoma,Intrahepatic Cholangiocarcinoma,Tubular Adenocarcinoma,Apocrine Adenocarcinoma,Adenocarcinoma In Situ,Gastroesophageal Junction Adenocarcinoma,Glioma,Leukemia, Acute Myeloid,Sporadic Breast Cancer,Trachea Leiomyoma,Bone Marrow Cancer,Periampullary Adenocarcinoma,Recurrent Respiratory Papillomatosis,Basal Cell Carcinoma,Cataract,High Grade Ependymoma,Mixed Glioma,Larynx Cancer,Laryngeal Benign Neoplasm,Rectal Disease,Papilloma,Horseshoe Kidney,Autonomic Nervous System Neoplasm,Kidney Cancer,Dilated Cardiomyopathy,Gastroesophageal Reflux,Pleural Cancer,Basal Cell Nevus Syndrome,Transitional Cell Carcinoma,Myoma,Hemangioblastoma,Bladder Cancer,Paronychia,Lung Disease,Ethmoid Sinus Adenocarcinoma,Soft Tissue Sarcoma,Thymus Gland Disease,Brain Cancer,Colonic Disease,Acute Interstitial Pneumonia,Hypopharynx Cancer,Mixed Cell Adenoma,Lung Adenoma,Diarrhea,Endometrial Adenocarcinoma,Laryngeal Squamous Cell Carcinoma,Oropharynx Cancer,Cervix Carcinoma,Oral Cavity Cancer,Keratinizing Squamous Cell Carcinoma,Basaloid Squamous Cell Carcinoma,Lip And Oral Cavity Cancer,Ovarian Cancer,Neonatal Inflammatory Skin And Bowel Disease,Supraglottis Cancer,Adenocarcinoma,In Situ Carcinoma,Testicular Cancer,Breast Ductal Carcinoma,Breast Malignant Phyllodes Tumor,Charcot-Marie-Tooth Disease,Mucinous Adenocarcinoma,Cervical Adenosquamous Carcinoma,Breast Carcinoma In Situ,Lung Carcinoma In Situ,Lymphoepithelioma-Like Carcinoma,Breast Cancer,Pleomorphic Carcinoma,Glioblastoma,Tonsil Cancer,Squamous Cell Carcinoma, Head And Neck,Malignant Astrocytoma,High Grade Glioma,Gliosarcoma,Giant Cell Glioblastoma,Anaplastic Astrocytoma,Colorectal Cancer,Interstitial Lung Disease,Peripheral Nervous System Disease,Nervous System Cancer,Familial Hypercholesterolemia,Squamous Blepharitis,Gallbladder Cancer,Hepatocellular Carcinoma,Anus Disease,Keratoacanthoma,Skin Papilloma,Inverted Papilloma,Salivary Gland Disease,Oligodendroglioma,Spinal Cord Oligodendroglioma,Malignant Peripheral Nerve Sheath Tumor,Microglandular Adenosis,Anus Cancer,Toxic Shock Syndrome,Tooth Disease,Rhabdomyosarcoma,Hepatitis C Virus,Biliary Tract Cancer,Tongue Disease,Thymoma,Thymus Cancer,Thymic Carcinoma,Prostatic Hypertrophy,Peutz-Jeghers Syndrome,Immunodeficiency 54,Mammary Paget'S Disease,Skin Carcinoma,Gastric Cancer,Breast Adenocarcinoma,Lymphangioma,Prostate Cancer,Disease Of Mental Health,Pancreatic Ductal Adenocarcinoma,Cholangiocarcinoma,Gallbladder Adenocarcinoma,Cerebral Ventricle Cancer,Pancreatic Ductal Carcinoma,Placental Site Trophoblastic Tumor,Ovarian Cystadenocarcinoma,Penile Disease,Pleural Disease,Mixed Cell Type Cancer,Central Nervous System Cancer,Respiratory System Disease,Cerebrum Cancer,Lung Benign Neoplasm,Integumentary System Disease,Skin Disease,Cervical Adenocarcinoma,Ovary Adenocarcinoma,Verrucous Carcinoma,Cervical Squamous Cell Carcinoma,Esophagus Verrucous Carcinoma,Childhood Medulloblastoma,Lynch Syndrome,Lung Squamous Cell Carcinoma,Hypotrichosis 13,Thyroid Gland Follicular Carcinoma,Renal Cell Carcinoma, Papillary, 1,Small Cell Cancer Of The Lung,Exanthem,Inflammatory Skin And Bowel Disease, Neonatal, 2,Esophageal Cancer,Respiratory System Benign Neoplasm,Gastrointestinal System Benign Neoplasm,Alveolar Soft Part Sarcoma,Small Cell Carcinoma,Tumor Predisposition Syndrome,Ewing Sarcoma,Lymphangioleiomyomatosis,Gastrointestinal Stromal Tumor,Colorectal Adenocarcinoma,Tongue Squamous Cell Carcinoma,Oral Squamous Cell Carcinoma,Pulmonary Adenocarcinoma In Situ,Large Cell Neuroendocrine Carcinoma,Bone Squamous Cell Carcinoma,Salivary Gland Carcinoma,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Renal Cell Carcinoma, Nonpapillary,Nasopharyngeal Carcinoma,Hypertension, Essential,Meningioma, Familial,Lymphoma,Pre-Malignant Neoplasm,Ductal Carcinoma In Situ,Estrogen-Receptor Positive Breast Cancer,Estrogen-Receptor Negative Breast Cancer,Progesterone-Receptor Negative Breast Cancer,Breast Benign Neoplasm,Cell Type Benign Neoplasm,Thoracic Benign Neoplasm,Brain Glioma,Pharynx Cancer,Gallbladder Disease,Leukemia, Chronic Lymphocytic,Amelogenesis Imperfecta, Type Ig,Li-Fraumeni Syndrome,Myeloma, Multiple,Medulloblastoma,Hepatoid Adenocarcinoma,Spinal Disease,Melanoma, Uveal,Retinitis Pigmentosa 11,Lung Cancer,Helicobacter Pylori Infection,Pancreatic Cancer |
5gnk_a | P00533 | ENSG00000146648 | EGFR | 99.00 | 7.20E-14 | 8.80E-18 | 126.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | RPS6KB1 STK14A |
Ribosomal protein S6 kinase beta-1 (S6K-beta-1) (S6K1) (EC 2.7.11.1) (70 kDa ribosomal protein S6 kinase 1) (P70S6K1) (p70-S6K 1) (Ribosomal protein S6 kinase I) (Serine/threonine-protein kinase 14A) (p70 ribosomal S6 kinase alpha) (p70 S6 kinase alpha) (p70 S6K-alpha) (p70 S6KA) |
2.7.11.1 | Homo sapiens | Mitral Valve Disease,Retinitis Pigmentosa,Cowden Syndrome,Pyriform Sinus Cancer,Cowden Syndrome 1,Placental Choriocarcinoma,Uterus Perivascular Epithelioid Cell Tumor,Subependymal Glioma,Benign Ependymoma,Leukemia, Acute Myeloid,Nephronophthisis,Kidney Angiomyolipoma,Aortic Disease,Skin Amelanotic Melanoma,Ovarian Cancer,Tuberous Sclerosis 2,Tuberous Sclerosis,Breast Cancer,Glioblastoma,Colorectal Cancer,Hepatocellular Carcinoma,Rhabdomyosarcoma,Acute Laryngopharyngitis,Gastric Cancer,Prostate Cancer,Disease Of Mental Health,Body Mass Index Quantitative Trait Locus 11,Type 2 Diabetes Mellitus,Diamond-Blackfan Anemia 20,Esophageal Cancer,Muscle Hypertrophy,Mantle Cell Lymphoma,Tuberous Sclerosis 1,Lymphangioleiomyomatosis,Leukodystrophy, Hypomyelinating, 12,Lung Cancer,Palmoplantar Keratoderma, Bothnian Type,Pancreatic Cancer |
3wf7_a | P23443 | ENSG00000108443 | RPS6KB1 | 99.00 | 7.40E-14 | 8.60E-18 | 130.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | CTR1 At5g03730 F17C15_150 |
Serine/threonine-protein kinase CTR1 (EC 2.7.11.1) (Protein CONSTITUTIVE TRIPLE RESPONSE1) |
2.7.11.1 | Arabidopsis thaliana | 3ppz_b | Q05609 | 98.90 | 1.40E-13 | 1.60E-17 | 128.50 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
YNL154C | YCK2 | SGDID:S000005098 | TTBK1 BDTK KIAA1855 |
Tau-tubulin kinase 1 (EC 2.7.11.1) (Brain-derived tau kinase) |
2.7.11.1 | Homo sapiens | Childhood-Onset Schizophrenia,Seckel Syndrome 4,Seckel Syndrome 8,Spinocerebellar Ataxia 11,Dystonia 12,Schizophrenia,Primary Autosomal Recessive Microcephaly |
4btk_a | Q5TCY1 | ENSG00000146216 | TTBK1 | 99.30 | 1.10E-16 | 1.30E-20 | 152.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | BIK1 At2g39660 F12L6.32 F17A14.3 |
Serine/threonine-protein kinase BIK1 (EC 2.7.11.1) (Protein BOTRYTIS-INDUCED KINASE 1) |
2.7.11.1 | Arabidopsis thaliana | 5tos_a | O48814 | 99.10 | 1.10E-14 | 1.30E-18 | 141.00 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
YNL154C | YCK2 | SGDID:S000005098 | FGFR1 BFGFR CEK FGFBR FLG FLT2 HBGFR |
Fibroblast growth factor receptor 1 (FGFR-1) (EC 2.7.10.1) (Basic fibroblast growth factor receptor 1) (BFGFR) (bFGF-R-1) (Fms-like tyrosine kinase 2) (FLT-2) (N-sam) (Proto-oncogene c-Fgr) (CD antigen CD331) |
2.7.10.1 | Homo sapiens | Adult Hepatocellular Carcinoma,Pancreatic Adenocarcinoma,Bone Disease,Bone Development Disease,Achondroplasia,Heart Disease,Fibrous Dysplasia,Endometrial Cancer,Apert Syndrome,Saethre-Chotzen Syndrome,Charge Syndrome,Pfeiffer Syndrome,Lymphoblastic Lymphoma,Myeloid And Lymphoid Neoplasms With Eosinophilia And Abnormalities Of Pdgfra, Pdgfrb, And Fgfr1,Retinitis Pigmentosa,Myeloid And Lymphoid Neoplasms Associated With Pdgfra Rearrangement,Myeloid And Lymphoid Neoplasms Associated With Fgfr1 Abnormalities,Brain Stem Glioma,Ossifying Fibroma,Melanoma,Chronic Eosinophilic Leukemia,Leukemia, Chronic Myeloid,Cleft Lip,Microform Holoprosencephaly,Hypogonadism,Dysostosis,B-Lymphoblastic Leukemia/Lymphoma,Neuroma,Synostosis,Rasopathy,Deafness, Autosomal Recessive 71,Congenital Hypogonadotropic Hypogonadism,Large Cell Carcinoma,Lung Large Cell Carcinoma,Holoprosencephaly,Osteochondroma,Cleft Lip/Palate,Nail Disorder, Nonsyndromic Congenital, 1,Myeloproliferative Neoplasm,Split Hand-Foot Malformation,Hypogonadotropic Hypogonadism,Semilobar Holoprosencephaly,Ankylosis,Radioulnar Synostosis,Cataract 30,Plagiocephaly,Lobar Holoprosencephaly,Leukemia,Syndromic Craniosynostosis,Craniosynostosis,Neuroblastoma,Mixed Phenotype Acute Leukemia,Pilomyxoid Astrocytoma,Pilocytic Astrocytoma,Cryptorchidism, Unilateral Or Bilateral,Hypereosinophilic Syndrome,Nevus, Epidermal,Acute Leukemia,Normosmic Congenital Hypogonadotropic Hypogonadism,Encephalocraniocutaneous Lipomatosis,Schimmelpenning-Feuerstein-Mims Syndrome,Glioma,Leukemia, Acute Myeloid,Phosphorus Metabolism Disease,Hematologic Cancer,Fibrolamellar Carcinoma,Leukemia, Acute Lymphoblastic,Hepatocellular Clear Cell Carcinoma,Chondroblastoma,Rosette-Forming Glioneuronal Tumor,Dysembryoplastic Neuroepithelial Tumor,Fgfr Craniosynostosis Syndromes,Sensorineural Hearing Loss,Choanal Atresia, Posterior,Infertility,Bladder Cancer,Primary Hypereosinophilic Syndrome,Megaesophagus,Osteoglophonic Dysplasia,Synovial Chondromatosis,Adenocarcinoma,Breast Carcinoma In Situ,Breast Cancer,Glioblastoma,Gliosarcoma,Giant Cell Glioblastoma,Colorectal Cancer,Isolated Trigonocephaly,Hepatocellular Carcinoma,8p11 Myeloproliferative Syndrome,Lipomatosis,Oligodendroglioma,Childhood Oligodendroglioma,Spinal Cord Oligodendroglioma,Adult Oligodendroglioma,Rhabdomyosarcoma,Hartsfield Syndrome,Muenke Syndrome,Pseudopterygium,Chromosome 8p11 Myeloproliferative Syndrome,Spotted Fever,Sarcoma,Cleft Palate, Isolated,Cleidocranial Dysplasia,Coloboma Of Macula,Gastric Cancer,Systemic Mastocytosis,Prostate Cancer,Disease Of Mental Health,Mastocytosis,Jackson-Weiss Syndrome,Body Mass Index Quantitative Trait Locus 11,Kallmann Syndrome,Crouzon Syndrome,Gastric Adenocarcinoma,Lung Squamous Cell Carcinoma,Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1,Bladder Urothelial Carcinoma,Holoprosencephaly 1,Septooptic Dysplasia,Hypophosphatemia,Antley-Bixler Syndrome,Esophageal Cancer,Hypertelorism, Microtia, Facial Clefting Syndrome,Odontochondrodysplasia,Orofacial Cleft,Chromosome 2q35 Duplication Syndrome,Tooth Agenesis,Thanatophoric Dysplasia, Type I,Trigonocephaly 1,Renal Hypodysplasia/Aplasia 1,Lymphoblastic Leukemia, Acute, With Lymphomatous Features,Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans,Salivary Gland Carcinoma,Hypochondroplasia,Hypogonadotropic Hypogonadism 7 With Or Without Anosmia,Lymphoma,Hypophosphatemic Rickets, X-Linked Dominant,Hypogonadotropic Hypogonadism 1 With Or Without Anosmia,Hypogonadotropic Hypogonadism 2 With Or Without Anosmia,Lacrimoauriculodentodigital Syndrome,Myelofibrosis,Medulloblastoma,Atypical Chronic Myeloid Leukemia,Neuroblastoma 1,C Syndrome,Tumoral Calcinosis, Hyperphosphatemic, Familial, 1,Lung Cancer,Oculoectodermal Syndrome,Cerebellar Hypoplasia/Atrophy, Epilepsy, And Global Developmental Delay,Pancreatic Cancer |
3tt0_a | P11362 | ENSG00000077782 | FGFR1 | 99.10 | 4.70E-15 | 5.30E-19 | 143.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | MAP3K8 COT ESTF |
Mitogen-activated protein kinase kinase kinase 8 (EC 2.7.11.25) (Cancer Osaka thyroid oncogene) (Proto-oncogene c-Cot) (Serine/threonine-protein kinase cot) (Tumor progression locus 2) (TPL-2) |
2.7.11.25 | Homo sapiens | Indolent Plasma Cell Myeloma,Paronychia,Skin Lipoma,Rheumatoid Arthritis,Lung Cancer |
4y85_b | P41279 | ENSG00000107968 | MAP3K8 | 99.00 | 4.40E-14 | 5.10E-18 | 132.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | STK3 KRS1 MST2 |
Serine/threonine-protein kinase 3 (EC 2.7.11.1) (Mammalian STE20-like protein kinase 2) (MST-2) (STE20-like kinase MST2) (Serine/threonine-protein kinase Krs-1) [Cleaved into: Serine/threonine-protein kinase 3 36kDa subunit (MST2/N); Serine/threonine-protein kinase 3 20kDa subunit (MST2/C)] |
2.7.11.1 | Homo sapiens | Non-Syndromic X-Linked Intellectual Disability |
4lg4_a | Q13188 | ENSG00000104375 | STK3 | 98.90 | 3.30E-13 | 3.90E-17 | 123.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | NEK7 |
Serine/threonine-protein kinase Nek7 (EC 2.7.11.1) (Never in mitosis A-related kinase 7) (NimA-related protein kinase 7) |
2.7.11.1 | Homo sapiens | Erysipeloid |
6gt1_b | Q8TDX7 | ENSG00000151414 | NEK7 | 98.90 | 2.30E-13 | 2.80E-17 | 124.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | PAK6 PAK5 |
Serine/threonine-protein kinase PAK 6 (EC 2.7.11.1) (PAK-5) (p21-activated kinase 6) (PAK-6) |
2.7.11.1 | Homo sapiens | 4ks7_a | Q9NQU5 | ENSG00000137843 | BUB1B-PAK6 | 98.90 | 2.40E-13 | 2.90E-17 | 123.60 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YNL154C | YCK2 | SGDID:S000005098 | Abl1 Abl |
Tyrosine-protein kinase ABL1 (EC 2.7.10.2) (Abelson murine leukemia viral oncogene homolog 1) (Abelson tyrosine-protein kinase 1) (Proto-oncogene c-Abl) (p150) |
2.7.10.2 | Mus musculus | 3kfa_b | P00520 | 99.10 | 1.50E-14 | 1.80E-18 | 130.90 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YNL154C | YCK2 | SGDID:S000005098 | FGFR4 JTK2 TKF |
Fibroblast growth factor receptor 4 (FGFR-4) (EC 2.7.10.1) (CD antigen CD334) |
2.7.10.1 | Homo sapiens | Functional Diarrhea,Gliomatosis Cerebri,Squamous Cell Carcinoma,Lung Cancer Susceptibility 3,Neuroendocrine Carcinoma,Adenoid Cystic Carcinoma,Rhabdomyosarcoma 2,Neuroma,Outlet Dysfunction Constipation,Constipation,Craniosynostosis,Nevus, Epidermal,Frontal Convexity Meningioma,Leber Plus Disease,Hepatocellular Clear Cell Carcinoma,Soft Tissue Sarcoma,Adenocarcinoma,Breast Cancer,Extrahepatic Cholestasis,Squamous Cell Carcinoma, Head And Neck,Anaplastic Astrocytoma,Colorectal Cancer,Hepatocellular Carcinoma,Rhabdomyosarcoma,Orbit Embryonal Rhabdomyosarcoma,Orbit Rhabdomyosarcoma,Prostate Cancer,Crouzon Syndrome,Lung Squamous Cell Carcinoma,Skeletal Muscle Cancer,Muscle Cancer,Odontochondrodysplasia,Thanatophoric Dysplasia, Type I,Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans,Hypochondroplasia,Hypophosphatemic Rickets, X-Linked Dominant,Lacrimoauriculodentodigital Syndrome,Parameningeal Embryonal Rhabdomyosarcoma,Pancreatic Cancer,Bjornstad Syndrome |
4qqt_a | P22455 | ENSG00000160867 | FGFR4 | 98.90 | 9.70E-14 | 1.10E-17 | 128.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | PTK2 FAK FAK1 |
Focal adhesion kinase 1 (FADK 1) (EC 2.7.10.2) (Focal adhesion kinase-related nonkinase) (FRNK) (p41/p43FRNK) (Protein-tyrosine kinase 2) (p125FAK) (pp125FAK) |
2.7.10.2 | Gallus gallus | 2j0l_a | Q00944 | 99.10 | 1.70E-14 | 2.00E-18 | 128.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YNL154C | YCK2 | SGDID:S000005098 | AAK1 KIAA1048 |
AP2-associated protein kinase 1 (EC 2.7.11.1) (Adaptor-associated kinase 1) |
2.7.11.1 | Homo sapiens | Parkinson Disease, Late-Onset,Cataract 8, Multiple Types,Hepatitis C Virus,Rabies |
5te0_a | Q2M2I8 | ENSG00000115977 | AAK1 | 99.00 | 5.80E-14 | 6.70E-18 | 132.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | CASK LIN2 |
Peripheral plasma membrane protein CASK (hCASK) (EC 2.7.11.1) (Calcium/calmodulin-dependent serine protein kinase) (Protein lin-2 homolog) |
2.7.11.1 | Homo sapiens | Cask-Related Disorders,Cerebellar Hypoplasia,Constipation,Congenital Nystagmus,Pathologic Nystagmus,Neurofibromatosis, Type I,Fraser Syndrome 1,Cask Disorders,Cerebellar Disease,Dystonia,Glucosephosphate Dehydrogenase Deficiency,Lobular Neoplasia,X-Linked Intellectual Disability, Najm Type,Cask-Related Intellectual Disability,Microcephaly,Hypertonia,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Fg Syndrome 4,Helsmoortel-Van Der Aa Syndrome,Aland Island Eye Disease,Developmental And Epileptic Encephalopathy 8,Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia,Anemia, Nonspherocytic Hemolytic, Due To G6pd Deficiency,Coffin-Siris Syndrome 1,Early Infantile Epileptic Encephalopathy,Opitz-Kaveggia Syndrome,Pontocerebellar Hypoplasia,Autism,Cerebellar Hypoplasia/Atrophy, Epilepsy, And Global Developmental Delay,Peho Syndrome |
3c0g_b | O14936 | ENSG00000147044 | CASK | 98.90 | 1.70E-13 | 1.90E-17 | 131.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | MET |
Hepatocyte growth factor receptor (HGF receptor) (EC 2.7.10.1) (HGF/SF receptor) (Proto-oncogene c-Met) (Scatter factor receptor) (SF receptor) (Tyrosine-protein kinase Met) |
2.7.10.1 | Homo sapiens | Pancreatic Adenocarcinoma,Mesothelioma, Malignant,Skin Melanoma,Familial Renal Papillary Carcinoma,Spinal Chordoma,Follicular Adenoma,Thyroid Gland Cancer,Peritoneal Mesothelioma,Lung Cancer Susceptibility 3,Occipital Lobe Neoplasm,Mucositis,Acral Lentiginous Melanoma,Chondrosarcoma,Chordoma,Chronic Erosive Gastritis,Melanoma,Gastroesophageal Adenocarcinoma,Thyroid Gland Anaplastic Carcinoma,Dedifferentiated Liposarcoma,Myxofibrosarcoma,Tongue Carcinoma,Hereditary Renal Cell Carcinoma,Clear Cell Renal Cell Carcinoma,Hepatoblastoma,Bile Duct Cancer,Tall Cell Variant Papillary Carcinoma,Doxorubicin Induced Cardiomyopathy,Differentiated Thyroid Carcinoma,Malignant Pleural Mesothelioma,Refractive Error,Ependymoblastoma,Neuroblastoma,Inherited Cancer-Predisposing Syndrome,Arthrogryposis, Distal, Type 1a,Glioma,Kidney Cancer,Lung Disease,Ovarian Clear Cell Adenocarcinoma,Hypopharynx Cancer,Ovarian Cancer,Adenocarcinoma,Breast Ductal Carcinoma,Breast Carcinoma In Situ,Breast Cancer,Glioblastoma,Squamous Cell Carcinoma, Head And Neck,High Grade Glioma,Colorectal Cancer,Papillary Carcinoma,Hepatocellular Carcinoma,Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb,Malignant Peripheral Nerve Sheath Tumor,Rhabdomyosarcoma,Biliary Tract Cancer,Gastric Cancer,Prostate Cancer,Papillary Thyroid Microcarcinoma,Cholangiocarcinoma,Microvascular Complications Of Diabetes 1,Lung Benign Neoplasm,Large Cell Medulloblastoma,Thyroid Gland Follicular Carcinoma,Autism 9,Renal Cell Carcinoma, Papillary, 1,Sarcoma, Synovial,Familial Mediterranean Fever, Autosomal Dominant,Barrett Esophagus,Distal Arthrogryposis,Alveolar Soft Part Sarcoma,Tumor Predisposition Syndrome,Vitreoretinopathy, Neovascular Inflammatory,Von Hippel-Lindau Syndrome,Salivary Gland Carcinoma,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Renal Cell Carcinoma, Nonpapillary,Autism Spectrum Disorder,Osteofibrous Dysplasia,Deafness, Autosomal Recessive 97,Inguinal Hernia,Medulloblastoma,Autism,Melanoma, Uveal,Pediatric Hepatocellular Carcinoma,Lung Cancer,Helicobacter Pylori Infection,Pancreatic Cancer |
4knb_a | P08581 | ENSG00000105976 | MET | 98.80 | 3.30E-13 | 4.00E-17 | 121.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | KDR FLK1 VEGFR2 |
Vascular endothelial growth factor receptor 2 (VEGFR-2) (EC 2.7.10.1) (Fetal liver kinase 1) (FLK-1) (Kinase insert domain receptor) (KDR) (Protein-tyrosine kinase receptor flk-1) (CD antigen CD309) |
2.7.10.1 | Homo sapiens | Psoriasis,Pancreatic Adenocarcinoma,Corneal Neovascularization,Mesothelioma, Malignant,Skin Melanoma,Pneumothorax,Heart Disease,Neovascular Glaucoma,Endocrine Gland Cancer,Retinal Vein Occlusion,Retinal Vascular Occlusion,Vascular Cancer,Retinitis Pigmentosa,Thyroid Gland Cancer,Ovarian Hyperstimulation Syndrome,Lung Cancer Susceptibility 3,Chronic Myelomonocytic Leukemia,Bone Cancer,Microvascular Complications Of Diabetes 5,Mast-Cell Leukemia,Melanoma,Malignant Ciliary Body Melanoma,Lung Non-Squamous Non-Small Cell Carcinoma,Diabetes Mellitus,Degeneration Of Macula And Posterior Pole,Macular Retinal Edema,Clear Cell Renal Cell Carcinoma,Septate Uterus,Primary Cutaneous B-Cell Lymphoma,Myocardial Infarction,Breast Angiosarcoma,Eye Degenerative Disease,Placenta Accreta,Cavernous Hemangioma,Neuroblastoma,Pilocytic Astrocytoma,Epithelioid Hemangioendothelioma,Arteriovenous Malformations Of The Brain,Olecranon Bursitis,Pulmonary Vein Stenosis,Retinal Vascular Disease,Gastroesophageal Junction Adenocarcinoma,Leukemia, Acute Myeloid,Capillary Disease,Hematologic Cancer,Hemangioma,Radiation Proctitis,Kidney Cancer,Leukostasis,Aortic Valve Disease 1,Hemangioblastoma,Bladder Cancer,Capillary Hemangioma,Heritable Pulmonary Arterial Hypertension,Retinal Artery Occlusion,Fundus Dystrophy,Parasitic Protozoa Infectious Disease,Kaposiform Hemangioendothelioma,Nodular Goiter,Background Diabetic Retinopathy,Endometriosis,Pediculus Humanus Capitis Infestation,Vein Disease,Bursitis,Ovarian Cancer,Hemangioma, Capillary Infantile,Adenocarcinoma,Pre-Eclampsia,Eye Disease,Cervical Adenosquamous Carcinoma,Breast Carcinoma In Situ,Breast Cancer,Glioblastoma,Squamous Cell Carcinoma, Head And Neck,Rosacea,High Grade Glioma,Gliosarcoma,Colorectal Cancer,Familial Hypercholesterolemia,Hepatocellular Carcinoma,Proctitis,Premature Menopause,8p11 Myeloproliferative Syndrome,Clopidogrel Resistance,Kuhnt-Junius Degeneration,Angiokeratoma Of Mibelli,Angiokeratoma Circumscriptum,Pheochromocytoma,Rhabdomyosarcoma,Ischemia,Cerebral Cavernous Malformations,Conjunctival Vascular Disease,Macular Degeneration, Age-Related, 1,Sarcoma,Hantavirus Pulmonary Syndrome,Fibrosarcoma Of Bone,Skin Carcinoma,Gastric Cancer,Lymphangioma,Mobitz Type Ii Atrioventricular Block,Prostate Cancer,Disease Of Mental Health,Coats Disease,Microvascular Complications Of Diabetes 1,Pulmonary Hypertension,Type 2 Diabetes Mellitus,Angiosarcoma,Drug-Induced Lupus Erythematosus,Placental Insufficiency,Thyroid Gland Follicular Carcinoma,Merkel Cell Carcinoma,Thyroid Gland Medullary Carcinoma,Renal Cell Carcinoma, Papillary, 1,Esophageal Cancer,Exudative Vitreoretinopathy 1,Tetralogy Of Fallot,Myelodysplastic Syndrome,Sorsby Fundus Dystrophy,Ewing Sarcoma,Gastrointestinal Stromal Tumor,Varicose Veins,Hirschsprung Disease 1,Limb Ischemia,Bone Squamous Cell Carcinoma,Renal Cell Carcinoma, Nonpapillary,Mucosal Melanoma,Hypertension, Essential,Lipoprotein Quantitative Trait Locus,Cardiovascular Organ Benign Neoplasm,Intussusception,Moyamoya Disease 1,Premature Ovarian Failure 1,Medulloblastoma,Lung Cancer,Pancreatic Cancer |
2xir_a | P35968 | ENSG00000128052 | KDR | 98.90 | 2.20E-13 | 2.60E-17 | 124.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | MERTK MER |
Tyrosine-protein kinase Mer (EC 2.7.10.1) (Proto-oncogene c-Mer) (Receptor tyrosine kinase MerTK) |
2.7.10.1 | Homo sapiens | Retinitis Pigmentosa,Degeneration Of Macula And Posterior Pole,Eye Degenerative Disease,Leber Plus Disease,Retinal Degeneration,Hereditary Retinal Dystrophy,Fundus Dystrophy,Retinal Disease,Achromatopsia,Usher Syndrome, Type Iiia,Choroid Disease,Stargardt Disease,Macular Degeneration, Age-Related, 1,Cone-Rod Dystrophy 2,Retinitis,Retinitis Pigmentosa 38,La Crosse Encephalitis,Usher Syndrome,Vitelliform Macular Dystrophy,Cone Dystrophy,Choroideremia,Leber Congenital Amaurosis 1,Leber Congenital Amaurosis 2,Systemic Lupus Erythematosus,Retinoschisis 1, X-Linked, Juvenile |
3brb_b | Q12866 | ENSG00000153208 | MERTK | 98.90 | 2.30E-13 | 2.70E-17 | 125.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | VRK3 |
Inactive serine/threonine-protein kinase VRK3 (Serine/threonine-protein pseudokinase VRK3) (Vaccinia-related kinase 3) |
Homo sapiens | Vaccinia |
2jii_a | Q8IV63 | ENSG00000105053 | VRK3 | 98.90 | 1.50E-13 | 1.80E-17 | 129.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YNL154C | YCK2 | SGDID:S000005098 | Ripk4 Ankrd3 Pkk |
Receptor-interacting serine/threonine-protein kinase 4 (EC 2.7.11.1) (Ankyrin repeat domain-containing protein 3) (PKC-associated protein kinase) (PKC-regulated protein kinase) |
2.7.11.1 | Mus musculus | 5wnj_a | Q9ERK0 | 99.00 | 5.10E-14 | 5.90E-18 | 132.90 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YNL154C | YCK2 | SGDID:S000005098 | PAK4 KIAA1142 |
Serine/threonine-protein kinase PAK 4 (EC 2.7.11.1) (p21-activated kinase 4) (PAK-4) |
2.7.11.1 | Homo sapiens | Polycystic Kidney Disease 3 With Or Without Polycystic Liver Disease |
4xbr_a | O96013 | ENSG00000130669 | PAK4 | 99.00 | 3.30E-14 | 3.80E-18 | 136.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | ERBB3 HER3 |
Receptor tyrosine-protein kinase erbB-3 (EC 2.7.10.1) (Proto-oncogene-like protein c-ErbB-3) (Tyrosine kinase-type cell surface receptor HER3) |
2.7.10.1 | Homo sapiens | Pancreatic Adenocarcinoma,Uterine Carcinosarcoma,Lung Cancer Susceptibility 3,Clear Cell Sarcoma,Mucinous Lung Adenocarcinoma,Neurogenic Bladder,Acute Erythroid Leukemia,Leukemia,Colonic Benign Neoplasm,Pilocytic Astrocytoma,Acoustic Neuroma,Periampullary Adenocarcinoma,Keratoconjunctivitis Sicca,Transitional Cell Carcinoma,Bladder Cancer,Retroperitoneal Leiomyosarcoma,Paronychia,Mixed Cell Adenoma,Vallecula Cancer,Ovarian Cancer,Gastric Fundus Cancer,Adenocarcinoma,Charcot-Marie-Tooth Disease,Breast Cancer,Glioblastoma,Squamous Cell Carcinoma, Head And Neck,Colorectal Cancer,Squamous Blepharitis,Gallbladder Cancer,Tooth Disease,Gastric Cancer,Breast Adenocarcinoma,Prostate Cancer,Cervical Cancer,Gastric Adenocarcinoma,Verrucous Carcinoma,Childhood Medulloblastoma,Schizophrenia,Ovary Transitional Cell Carcinoma,Bladder Urothelial Carcinoma,Erythroleukemia, Familial,Esophageal Cancer,Ductal Carcinoma In Situ,Estrogen-Receptor Positive Breast Cancer,Lethal Congenital Contracture Syndrome 2,Lethal Congenital Contracture Syndrome 1,Medulloblastoma,Lethal Congenital Contracture Syndrome,Lung Cancer,Pancreatic Cancer |
3kex_a | P21860 | ENSG00000065361 | ERBB3 | 98.90 | 3.20E-13 | 3.70E-17 | 125.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | EPHB4 HTK MYK1 TYRO11 |
Ephrin type-B receptor 4 (EC 2.7.10.1) (Hepatoma transmembrane kinase) (Tyrosine-protein kinase TYRO11) |
2.7.10.1 | Homo sapiens | Endometrial Cancer,Liver Carcinoma In Situ,Capillary Malformation-Arteriovenous Malformation 1,Skin Angiosarcoma,Parkes Weber Syndrome,Brain Stem Astrocytic Neoplasm,Hereditary Hemorrhagic Telangiectasia,Lymphatic Malformation 7,Ovarian Cancer,Breast Cancer,Squamous Cell Carcinoma, Head And Neck,Weber Syndrome,Colorectal Cancer,Arteriovenous Malformation,Microvascular Complications Of Diabetes 1,Capillary Malformation-Arteriovenous Malformation 2,Tetralogy Of Fallot,Cardiovascular Organ Benign Neoplasm,Hennekam Syndrome |
6fnk_a | P54760 | ENSG00000196411 | EPHB4 | 99.00 | 4.50E-14 | 5.40E-18 | 128.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YNL154C | YCK2 | SGDID:S000005098 | CAMK4 CAMK CAMK-GR CAMKIV |
Calcium/calmodulin-dependent protein kinase type IV (CaMK IV) (EC 2.7.11.17) (CaM kinase-GR) |
2.7.11.17 | Homo sapiens | Lung Large Cell Carcinoma,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Crouzon Syndrome With Acanthosis Nigricans,Systemic Lupus Erythematosus,Gingival Fibromatosis |
2w4o_a | Q16566 | ENSG00000152495 | CAMK4 | 98.90 | 9.40E-14 | 1.10E-17 | 133.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |