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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YLR253W | MCP2 | SGDID:S000004243 | rio2 AF_2426 |
RIO-type serine/threonine-protein kinase Rio2 (AfRio2) (EC 2.7.11.1) |
2.7.11.1 | Archaeoglobus fulgidus | 1zao_a | O30245 | 99.10 | 2.10E-14 | 1.80E-18 | 142.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YLR253W | MCP2 | SGDID:S000004243 | 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 | 98.80 | 1.30E-12 | 1.20E-16 | 126.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YLR253W | MCP2 | SGDID:S000004243 | 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 | 99.20 | 1.00E-15 | 9.30E-20 | 158.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YLR253W | MCP2 | SGDID:S000004243 | MAP4K3 RAB8IPL1 |
Mitogen-activated protein kinase kinase kinase kinase 3 (EC 2.7.11.1) (Germinal center kinase-related protein kinase) (GLK) (MAPK/ERK kinase kinase kinase 3) (MEK kinase kinase 3) (MEKKK 3) |
2.7.11.1 | Homo sapiens | Adult-Onset Still'S Disease |
5j5t_a | Q8IVH8 | ENSG00000011566 | MAP4K3 | 98.70 | 2.70E-12 | 2.40E-16 | 130.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YLR253W | MCP2 | SGDID:S000004243 | 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 | 99.50 | 9.20E-19 | 7.70E-23 | 177.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YLR253W | MCP2 | SGDID:S000004243 | 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 | 98.80 | 7.70E-13 | 7.00E-17 | 137.20 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YLR253W | MCP2 | SGDID:S000004243 | 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 |
5otf_a | Q9Y5S2 | ENSG00000198752 | CDC42BPB | 98.70 | 2.90E-12 | 2.60E-16 | 132.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YLR253W | MCP2 | SGDID:S000004243 | 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 | 98.70 | 2.80E-12 | 2.60E-16 | 122.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YLR253W | MCP2 | SGDID:S000004243 | 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 | 98.70 | 2.30E-12 | 2.20E-16 | 126.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YLR253W | MCP2 | SGDID:S000004243 | 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 | 98.80 | 1.40E-12 | 1.20E-16 | 130.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YLR253W | MCP2 | SGDID:S000004243 | 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 | 98.70 | 2.00E-12 | 1.80E-16 | 129.30 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YLR253W | MCP2 | SGDID:S000004243 | Rv3197 |
Rv3197 |
Mycobacterium tuberculosis | 5yk0_a | O53343 | 99.90 | 8.00E-29 | 6.90E-33 | 264.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YLR253W | MCP2 | SGDID:S000004243 | 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 | 98.70 | 2.10E-12 | 1.90E-16 | 127.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YLR253W | MCP2 | SGDID:S000004243 | 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 | 98.70 | 2.10E-12 | 1.90E-16 | 130.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YLR253W | MCP2 | SGDID:S000004243 | RIOK1 RIO1 |
Serine/threonine-protein kinase RIO1 (EC 2.7.11.1) (EC 3.6.3.-) (RIO kinase 1) |
2.7.11.1,3.6.3.-, | Homo sapiens | Cecum Adenocarcinoma,Cecum Carcinoma,Alcohol-Related Neurodevelopmental Disorder |
4otp_a | Q9BRS2 | 98.90 | 2.40E-13 | 2.00E-17 | 139.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YLR253W | MCP2 | SGDID:S000004243 | 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 | 98.80 | 9.20E-13 | 8.20E-17 | 134.90 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
YLR253W | MCP2 | SGDID:S000004243 | 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 | 4d4r_a | Q00944 | 98.70 | 2.70E-12 | 2.50E-16 | 122.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YLR253W | MCP2 | SGDID:S000004243 | 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 | 98.70 | 3.00E-12 | 2.80E-16 | 132.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YLR253W | MCP2 | SGDID:S000004243 | COQ8A ADCK3 CABC1 PP265 |
Atypical kinase COQ8A, mitochondrial (EC 2.7.-.-) (Chaperone activity of bc1 complex-like) (Chaperone-ABC1-like) (Coenzyme Q protein 8A) (aarF domain-containing protein kinase 3) |
2.7.-.- | Homo sapiens | Mitochondrial Encephalomyopathy,Nephrotic Syndrome,Pathologic Nystagmus,Chronic Progressive External Ophthalmoplegia,Leigh Syndrome With Nephrotic Syndrome,Cerebellar Disease,Mitochondrial Disorders,Spinocerebellar Ataxia, Autosomal Recessive 14,Cardiofaciocutaneous Syndrome 1,Multiple Acyl-Coa Dehydrogenase Deficiency,Aceruloplasminemia,Mental Retardation, X-Linked, With Cerebellar Hypoplasia And Distinctive Facial Appearance,Spinocerebellar Ataxia, Autosomal Recessive 8,Coenzyme Q10 Deficiency, Primary, 4,Coenzyme Q10 Deficiency, Primary, 7,Coenzyme Q10 Deficiency Disease,Marinesco-Sjogren Syndrome,Autosomal Recessive Cerebellar Ataxia,Hereditary Ataxia,Spastic Ataxia,Joubert Syndrome 17,Coenzyme Q10 Deficiency, Primary, 6,Coenzyme Q10 Deficiency, Primary, 5,Spastic Paraplegia 7, Autosomal Recessive,Coenzyme Q10 Deficiency, Primary, 1,Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis,Mitochondrial Complex I Deficiency, Nuclear Type 1,Ataxia, Early-Onset, With Oculomotor Apraxia And Hypoalbuminemia,Kearns-Sayre Syndrome,Leigh Syndrome |
4ped_a | Q8NI60 | ENSG00000163050 | COQ8A | 99.90 | 5.20E-31 | 4.40E-35 | 277.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YLR253W | MCP2 | SGDID:S000004243 | CTHT_0033330 |
CTHT_0033330 |
2.7.11.1 | Chaetomium thermophilum | 4gyi_a | G0S5R3 | 99.30 | 1.10E-16 | 9.00E-21 | 167.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YLR253W | MCP2 | SGDID:S000004243 | RIO2 YNL207W N1342 |
Serine/threonine-protein kinase RIO2 (EC 2.7.11.1) |
2.7.11.1 | Saccharomyces cerevisiae | 6fai_l | P40160 | 99.30 | 5.80E-16 | 4.80E-20 | 163.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YLR253W | MCP2 | SGDID:S000004243 | 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 | 98.90 | 2.40E-13 | 2.20E-17 | 137.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YLR253W | MCP2 | SGDID:S000004243 | 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 | 98.80 | 7.60E-13 | 6.80E-17 | 134.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YLR253W | MCP2 | SGDID:S000004243 | 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 |
4ase_a | P35968 | ENSG00000128052 | KDR | 98.70 | 2.40E-12 | 2.10E-16 | 129.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YLR253W | MCP2 | SGDID:S000004243 | 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 | 98.80 | 1.40E-12 | 1.20E-16 | 129.80 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YLR253W | MCP2 | SGDID:S000004243 | 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 |
2q0n_a | O96013 | ENSG00000130669 | PAK4 | 98.70 | 2.10E-12 | 1.90E-16 | 126.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YLR253W | MCP2 | SGDID:S000004243 | 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 | 98.70 | 2.00E-12 | 1.80E-16 | 129.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YLR253W | MCP2 | SGDID:S000004243 | GRK2 ADRBK1 BARK BARK1 |
Beta-adrenergic receptor kinase 1 (Beta-ARK-1) (EC 2.7.11.15) (G-protein coupled receptor kinase 2) |
2.7.11.15 | Homo sapiens | Heart Disease,Alzheimer Disease,Myocardial Infarction,Exudative Vitreoretinopathy 5,Colorectal Cancer,Disease Of Mental Health,Hypertension, Essential |
3v5w_a | P25098 | ENSG00000173020 | GRK2 | 99.30 | 6.30E-16 | 5.00E-20 | 172.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YLR253W | MCP2 | SGDID:S000004243 | RIOK2 RIO2 |
Serine/threonine-protein kinase RIO2 (EC 2.7.11.1) (RIO kinase 2) |
2.7.11.1 | Homo sapiens | Diamond-Blackfan Anemia,Cecum Adenocarcinoma,Strongyloidiasis,Cecum Carcinoma,Alcohol-Related Neurodevelopmental Disorder |
6fdm_a | Q9BVS4 | ENSG00000058729 | RIOK2 | 99.40 | 2.20E-17 | 1.90E-21 | 166.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YLR253W | MCP2 | SGDID:S000004243 | 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 | 98.80 | 8.30E-13 | 7.40E-17 | 136.80 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
YLR253W | MCP2 | SGDID:S000004243 | 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 | 98.80 | 1.30E-12 | 1.20E-16 | 125.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YLR253W | MCP2 | SGDID:S000004243 | 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 | 99.20 | 1.50E-15 | 1.30E-19 | 154.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YLR253W | MCP2 | SGDID:S000004243 | 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 | 98.80 | 1.60E-12 | 1.40E-16 | 130.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |