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 |
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YPL236C | ENV7 | SGDID:S000006157 | 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 | 100.00 | 6.40E-36 | 7.60E-40 | 261.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YPL236C | ENV7 | SGDID:S000006157 | 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 | 99.90 | 4.60E-30 | 7.10E-34 | 198.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YPL236C | ENV7 | SGDID:S000006157 | STK16 MPSK1 PKL12 TSF1 |
Serine/threonine-protein kinase 16 (EC 2.7.11.1) (Myristoylated and palmitoylated serine/threonine-protein kinase) (MPSK) (Protein kinase PKL12) (TGF-beta-stimulated factor 1) (TSF-1) (Tyrosine-protein kinase STK16) (EC 2.7.10.2) (hPSK) |
2.7.10.2,2.7.11.1, | Homo sapiens | Diffuse Mesangial Sclerosis,Atrial Septal Defect 6 |
2buj_a | O75716 | ENSG00000115661 | STK16 | 99.90 | 8.70E-33 | 1.30E-36 | 219.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YPL236C | ENV7 | SGDID:S000006157 | 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 | 99.90 | 5.20E-30 | 7.40E-34 | 216.30 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
YPL236C | ENV7 | SGDID:S000006157 | BMP2K BIKE HRIHFB2017 |
BMP-2-inducible protein kinase (BIKe) (EC 2.7.11.1) |
2.7.11.1 | Homo sapiens | Myopia |
4w9w_a | Q9NSY1 | ENSG00000138756 | BMP2K | 99.90 | 1.60E-31 | 2.40E-35 | 210.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YPL236C | ENV7 | SGDID:S000006157 | GAK |
Cyclin-G-associated kinase (EC 2.7.11.1) |
2.7.11.1 | Homo sapiens | Parkinson Disease, Late-Onset,Cataract 8, Multiple Types,Postencephalitic Parkinson Disease,Parkinson Disease 15, Autosomal Recessive Early-Onset |
4o38_a | O14976 | ENSG00000178950 | GAK | 99.90 | 2.80E-31 | 4.20E-35 | 212.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YPL236C | ENV7 | SGDID:S000006157 | 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 | 99.90 | 4.90E-31 | 7.70E-35 | 202.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YPL236C | ENV7 | SGDID:S000006157 | 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 | 99.90 | 2.10E-30 | 3.30E-34 | 200.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YPL236C | ENV7 | SGDID:S000006157 | 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 |
4iva_a | O60674 | ENSG00000096968 | JAK2 | 99.90 | 2.10E-30 | 3.30E-34 | 202.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YPL236C | ENV7 | SGDID:S000006157 | Tyk2 |
Non-receptor tyrosine-protein kinase TYK2 (EC 2.7.10.2) |
2.7.10.2 | Mus musculus | 4e1z_a | Q9R117 | 99.90 | 6.30E-30 | 9.70E-34 | 198.10 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YPL236C | ENV7 | SGDID:S000006157 | BRI1 At4g39400 F23K16.30 |
Protein BRASSINOSTEROID INSENSITIVE 1 (AtBRI1) (EC 2.7.10.1) (EC 2.7.11.1) (Brassinosteroid LRR receptor kinase) |
2.7.10.1,2.7.11.1, | Arabidopsis thaliana | 5lpy_a | O22476 | 99.90 | 6.90E-30 | 1.00E-33 | 201.50 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
YPL236C | ENV7 | SGDID:S000006157 | 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 |
4wsq_a | Q2M2I8 | ENSG00000115977 | AAK1 | 99.90 | 5.60E-30 | 8.40E-34 | 203.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |