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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YKL171W | NNK1 | SGDID:S000001654 | CHEK1 CHK1 |
Serine/threonine-protein kinase Chk1 (EC 2.7.11.1) (CHK1 checkpoint homolog) (Cell cycle checkpoint kinase) (Checkpoint kinase-1) |
2.7.11.1 | Homo sapiens | Tongue Carcinoma,Neuroblastoma,Leukemia, Acute Myeloid,Sporadic Breast Cancer,Cerebellar Disease,Ovarian Cancer,Breast Cancer,Colorectal Cancer,Microcephaly,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Retinoblastoma,Esophageal Cancer,Seckel Syndrome,Mantle Cell Lymphoma,Pigmentary Disorder, Reticulate, With Systemic Manifestations, X-Linked,Ovarian Clear Cell Carcinoma,Autosomal Recessive Cerebellar Ataxia,Li-Fraumeni Syndrome,Ataxia-Telangiectasia,Medulloblastoma,Primary Autosomal Recessive Microcephaly,Lung Cancer |
2e9v_b | O14757 | ENSG00000149554 | CHEK1 | 99.40 | 3.10E-17 | 4.00E-21 | 154.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.40 | 6.60E-18 | 7.90E-22 | 169.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.40 | 3.20E-17 | 3.80E-21 | 164.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.40 | 6.30E-18 | 7.60E-22 | 169.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.40 | 1.90E-17 | 2.20E-21 | 168.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | GSK3B |
Glycogen synthase kinase-3 beta (GSK-3 beta) (EC 2.7.11.26) (Serine/threonine-protein kinase GSK3B) (EC 2.7.11.1) |
2.7.11.26 | Homo sapiens | Liver Disease,Endometrial Cancer,Epilepsy,Polycystic Kidney Disease,Diabetes Mellitus,Alzheimer Disease,Major Depressive Disorder,Neuroblastoma,Cervical Non-Keratinizing Squamous Cell Carcinoma,Barbiturate Dependence,Alzheimer Disease 9,Dementia,Fallopian Tube Serous Adenocarcinoma,Breast Cancer,Parkinson Disease, Late-Onset,Colorectal Cancer,Parkinson Disease 1, Autosomal Dominant,Hepatocellular Carcinoma,Bipolar Disorder,Gastric Cancer,Prostate Cancer,Disease Of Mental Health,Type 2 Diabetes Mellitus,Schizophrenia,Ophthalmomyiasis,Familial Adenomatous Polyposis,Severe Congenital Neutropenia,Aneurysmal Bone Cysts,Attention Deficit-Hyperactivity Disorder,Medulloblastoma,Frontotemporal Dementia,Pancreatic Cancer |
1j1b_b | P49841 | ENSG00000082701 | GSK3B | 99.30 | 9.60E-17 | 1.10E-20 | 165.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | roco4 DDB_G0288251 |
Probable serine/threonine-protein kinase roco4 (EC 2.7.11.1) (Ras of complex proteins and C-terminal of roc 4) |
2.7.11.1 | Dictyostelium discoideum | 4f1m_a | Q6XHB2 | 99.40 | 4.50E-17 | 5.80E-21 | 154.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKL171W | NNK1 | SGDID:S000001654 | PTSG_10090 |
PTSG_10090 |
2.7.11.17 | Salpingoeca rosetta | 5ig1_b | F2UPG5 | 99.30 | 6.90E-17 | 8.10E-21 | 163.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.40 | 2.80E-17 | 3.40E-21 | 166.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.30 | 8.90E-17 | 1.10E-20 | 153.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | MAP4K1 HPK1 |
Mitogen-activated protein kinase kinase kinase kinase 1 (EC 2.7.11.1) (Hematopoietic progenitor kinase) (MAPK/ERK kinase kinase kinase 1) (MEK kinase kinase 1) (MEKKK 1) |
2.7.11.1 | Homo sapiens | 6cqe_a | Q92918 | ENSG00000104814 | MAP4K1 | 99.30 | 9.60E-17 | 1.20E-20 | 154.40 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YKL171W | NNK1 | SGDID:S000001654 | unc-43 K11E8.1 |
Calcium/calmodulin-dependent protein kinase type II (CaM kinase II) (EC 2.7.11.17) (Uncoordinated protein 43) |
2.7.11.17 | Caenorhabditis elegans | 2bdw_b | O62305 | 99.40 | 4.90E-17 | 5.80E-21 | 165.30 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | |||
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.30 | 6.40E-17 | 7.80E-21 | 160.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | Pto |
Pto |
Solanum pimpinellifolium | 2qkw_b | Q40234 | 99.30 | 6.10E-17 | 7.50E-21 | 159.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.30 | 1.00E-16 | 1.30E-20 | 155.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | BN1205_040370 TGVEG_207820 |
BN1205_040370 TGVEG_207820 |
2.7.11.24 | Toxoplasma gondii | 3rp9_a | B6KP12 | 99.30 | 1.30E-16 | 1.50E-20 | 166.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.40 | 1.80E-17 | 2.20E-21 | 158.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.30 | 7.50E-17 | 8.90E-21 | 159.70 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.30 | 6.40E-17 | 7.70E-21 | 160.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.40 | 1.30E-17 | 1.60E-21 | 171.20 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.30 | 8.60E-17 | 1.00E-20 | 160.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | ROCK2 |
Rho-associated protein kinase 2 (EC 2.7.11.1) (Rho-associated, coiled-coil-containing protein kinase 2) (Rho-associated, coiled-coil-containing protein kinase II) (ROCK-II) (p164 ROCK-2) |
2.7.11.1 | Bos taurus | 2f2u_b | Q28021 | 99.40 | 3.90E-17 | 4.50E-21 | 169.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.30 | 7.90E-17 | 1.00E-20 | 155.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.30 | 8.00E-17 | 1.00E-20 | 154.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.30 | 1.20E-16 | 1.50E-20 | 151.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.40 | 1.10E-17 | 1.30E-21 | 170.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.40 | 2.70E-17 | 3.20E-21 | 167.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | 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 |
6jpj_a | P22455 | ENSG00000160867 | FGFR4 | 99.30 | 1.10E-16 | 1.30E-20 | 155.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.30 | 9.50E-17 | 1.10E-20 | 163.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | WNK3 KIAA1566 PRKWNK3 |
Serine/threonine-protein kinase WNK3 (EC 2.7.11.1) (Protein kinase lysine-deficient 3) (Protein kinase with no lysine 3) |
2.7.11.1 | Homo sapiens | Bartter Disease,Renal Tubular Transport Disease,Pseudohypoaldosteronism,Agenesis Of The Corpus Callosum With Peripheral Neuropathy,Arthrogryposis, Distal, Type 3,Liddle Syndrome 1,Hypomagnesemia 4, Renal,Distal Arthrogryposis,Hypertension, Essential,Syndromic X-Linked Intellectual Disability Siderius Type,Gitelman Syndrome |
5o2c_a | Q9BYP7 | ENSG00000196632 | WNK3 | 99.30 | 6.80E-17 | 7.90E-21 | 166.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | PHKG1 PHKG |
Phosphorylase b kinase gamma catalytic chain, skeletal muscle/heart isoform (EC 2.7.11.19) (Phosphorylase kinase subunit gamma-1) (Serine/threonine-protein kinase PHKG1) (EC 2.7.11.1) (EC 2.7.11.26) |
2.7.11.1,2.7.11.19,2.7.11.26 | Oryctolagus cuniculus | 2phk_a | P00518 | 99.30 | 1.10E-16 | 1.40E-20 | 151.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.30 | 9.70E-17 | 1.20E-20 | 152.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.40 | 4.10E-17 | 4.80E-21 | 166.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | PLK4 SAK STK18 |
Serine/threonine-protein kinase PLK4 (EC 2.7.11.21) (Polo-like kinase 4) (PLK-4) (Serine/threonine-protein kinase 18) (Serine/threonine-protein kinase Sak) |
2.7.11.21 | Homo sapiens | Congenital Nervous System Abnormality,Autosomal Recessive Chorioretinopathy-Microcephaly Syndrome,Colorectal Cancer,Microcephaly,Seckel Syndrome,Microcephaly And Chorioretinopathy, Autosomal Recessive, 2,Isolated Growth Hormone Deficiency,Primary Autosomal Recessive Microcephaly,Joubert Syndrome 1,Isolated Growth Hormone Deficiency, Type Ia |
4jxf_a | O00444 | ENSG00000142731 | PLK4 | 99.30 | 7.30E-17 | 9.20E-21 | 152.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.40 | 6.50E-18 | 7.90E-22 | 170.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | MELK KIAA0175 |
Maternal embryonic leucine zipper kinase (hMELK) (EC 2.7.11.1) (Protein kinase Eg3) (pEg3 kinase) (Protein kinase PK38) (hPK38) (Tyrosine-protein kinase MELK) (EC 2.7.10.2) |
2.7.10.2 | Homo sapiens | Colorectal Cancer |
5k00_a | Q14680 | ENSG00000165304 | MELK | 99.30 | 8.10E-17 | 9.60E-21 | 162.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | PBK TOPK |
Lymphokine-activated killer T-cell-originated protein kinase (EC 2.7.12.2) (Cancer/testis antigen 84) (CT84) (MAPKK-like protein kinase) (Nori-3) (PDZ-binding kinase) (Spermatogenesis-related protein kinase) (SPK) (T-LAK cell-originated protein kinase) |
2.7.12.2 | Homo sapiens | Fuchs' Endothelial Dystrophy,Hematologic Cancer,Plexiform Neurofibroma,Cicatricial Entropion,Malignant Peripheral Nerve Sheath Tumor,Corneal Edema |
5j0a_b | Q96KB5 | ENSG00000168078 | PBK | 99.40 | 3.80E-17 | 4.80E-21 | 156.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | STK17B DRAK2 |
Serine/threonine-protein kinase 17B (EC 2.7.11.1) (DAP kinase-related apoptosis-inducing protein kinase 2) |
2.7.11.1 | Homo sapiens | Colon Squamous Cell Carcinoma |
3lm5_a | O94768 | ENSG00000081320 | STK17B | 99.30 | 9.30E-17 | 1.10E-20 | 160.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | 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 | 3.10E-17 | 3.70E-21 | 163.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.40 | 6.90E-18 | 8.70E-22 | 165.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.40 | 2.80E-17 | 3.40E-21 | 163.40 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YKL171W | NNK1 | SGDID:S000001654 | Prag1 Pragmin |
Inactive tyrosine-protein kinase PRAG1 (PEAK1-related kinase-activating pseudokinase 1) (Pragma of Rnd2) |
Rattus norvegicus | 6ewx_a | D3ZMK9 | 99.30 | 9.40E-17 | 1.00E-20 | 172.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.30 | 8.50E-17 | 9.90E-21 | 165.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | CAMK2D CAMKD |
Calcium/calmodulin-dependent protein kinase type II subunit delta (CaM kinase II subunit delta) (CaMK-II subunit delta) (EC 2.7.11.17) |
2.7.11.17 | Homo sapiens | Dilated Cardiomyopathy,Cardiomyopathy, Dilated, 1dd |
2wel_a | Q13557 | ENSG00000145349 | CAMK2D | 99.40 | 1.20E-17 | 1.50E-21 | 165.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | DYRK2 |
Dual specificity tyrosine-phosphorylation-regulated kinase 2 (EC 2.7.12.1) |
2.7.12.1 | Homo sapiens | 4azf_a | Q92630 | ENSG00000127334 | DYRK2 | 99.30 | 7.00E-17 | 8.10E-21 | 168.40 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.50 | 2.00E-19 | 2.40E-23 | 187.20 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | |||
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.40 | 3.10E-17 | 3.80E-21 | 164.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.40 | 9.80E-18 | 1.20E-21 | 167.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | Taok2 Tao2 |
Serine/threonine-protein kinase TAO2 (EC 2.7.11.1) (Thousand and one amino acid protein 2) |
2.7.11.1 | Rattus norvegicus | 1u5r_b | Q9JLS3 | 99.30 | 9.00E-17 | 1.10E-20 | 162.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.80 | 4.50E-26 | 4.60E-30 | 237.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.40 | 2.40E-17 | 3.00E-21 | 165.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.30 | 6.70E-17 | 8.70E-21 | 152.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | P0510F09.27 |
P0510F09.27 |
Oryza sativa | 3sv0_a | Q8LR51 | 99.30 | 9.00E-17 | 9.60E-21 | 174.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YKL171W | NNK1 | SGDID:S000001654 | 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 |
5ng3_a | O43353 | ENSG00000104312 | RIPK2 | 99.30 | 1.10E-16 | 1.40E-20 | 154.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | HRR25 YPL204W |
Casein kinase I homolog HRR25 (EC 2.7.11.1) |
2.7.11.1 | Saccharomyces cerevisiae | 5cyz_a | P29295 | 99.30 | 5.30E-17 | 6.30E-21 | 166.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.40 | 3.30E-17 | 4.10E-21 | 158.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.40 | 1.10E-17 | 1.40E-21 | 167.60 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | |||
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.30 | 7.80E-17 | 9.80E-21 | 154.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | 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 | 99.30 | 6.80E-17 | 8.50E-21 | 156.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YKL171W | NNK1 | SGDID:S000001654 | VRK3 |
Inactive serine/threonine-protein kinase VRK3 (Serine/threonine-protein pseudokinase VRK3) (Vaccinia-related kinase 3) |
Homo sapiens | Vaccinia |
2jii_a | Q8IV63 | ENSG00000105053 | VRK3 | 99.30 | 1.10E-16 | 1.30E-20 | 160.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |