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AnalogYeast
One stop shop for finding analogs for your favorite yeast protein

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YGR092W DBF2 / SGDID:S000003324
SGD CSV
Disease Associated
Homo Sapiens
Mus Musculus
Danio Rerio
Drosophila Melanogaster
Caenorhabditis Elegans
Arabidopsis Thaliana
Escherichia Coli
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
YGR092W DBF2 SGDID:S000003324
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
3zos_b Q08345 ENSG00000204580 DDR1 99.40 3.10E-17 3.10E-21 160.00 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 99.70 1.30E-22 1.20E-26 208.70 0 0 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 2.90E-17 3.00E-21 157.90 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
PKN1 PAK1 PKN PRK1 PRKCL1
Serine/threonine-protein kinase N1 (EC 2.7.11.13) (Protease-activated kinase 1) (PAK-1) (Protein kinase C-like 1) (Protein kinase C-like PKN) (Protein kinase PKN-alpha) (Protein-kinase C-related kinase 1) (Serine-threonine protein kinase N)
2.7.11.13 Homo sapiens
4otd_a Q16512 ENSG00000123143 PKN1 99.60 2.70E-20 2.70E-24 184.60 0 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 9.40E-18 9.40E-22 166.60 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
STK38 NDR1
Serine/threonine-protein kinase 38 (EC 2.7.11.1) (NDR1 protein kinase) (Nuclear Dbf2-related kinase 1)
2.7.11.1 Homo sapiens
Myeloproliferative Syndrome, Transient,Wilson-Turner X-Linked Mental Retardation Syndrome
6bxi_a Q15208 ENSG00000112079 STK38 99.70 3.60E-21 3.70E-25 191.00 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 99.50 5.40E-19 5.40E-23 176.20 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
PRKG1 PRKG1B PRKGR1A PRKGR1B
cGMP-dependent protein kinase 1 (cGK 1) (cGK1) (EC 2.7.11.12) (cGMP-dependent protein kinase I) (cGKI)
2.7.11.12 Homo sapiens
Myopathy,Impotence,Connective Tissue Disease,Diabetes Mellitus,Aortic Dissection,Alzheimer Disease,Familial Thoracic Aortic Aneurysm And Aortic Dissection,Cystic Fibrosis,Aortic Disease,Aortic Valve Disease 1,Heritable Thoracic Aortic Disease,Hemolytic Anemia,Non-Proliferative Fibrocystic Change Of The Breast,Aneurysm,Aortic Aneurysm, Familial Thoracic 8,Disease Of Mental Health,Pulmonary Hypertension,Body Mass Index Quantitative Trait Locus 11,Aortic Aneurysm,Loeys-Dietz Syndrome,Immune Deficiency Disease,Myelodysplastic Syndrome,Attention Deficit-Hyperactivity Disorder,Aortic Aneurysm, Familial Thoracic 1,Hypertension, Essential,Sexual Disorder
6bg2_a Q13976 ENSG00000185532 PRKG1 99.60 1.10E-20 1.10E-24 189.30 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 2.60E-17 2.60E-21 162.00 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
ROCK1
Rho-associated protein kinase 1 (EC 2.7.11.1) (Renal carcinoma antigen NY-REN-35) (Rho-associated, coiled-coil-containing protein kinase 1) (Rho-associated, coiled-coil-containing protein kinase I) (ROCK-I) (p160 ROCK-1) (p160ROCK)
2.7.11.1 Homo sapiens
Coronary Artery Vasospasm,Ocular Hyperemia,Breast Cancer,Pediatric Osteosarcoma,Hutchinson-Gilford Progeria Syndrome,Tetralogy Of Fallot,Hypertension, Essential,Lung Cancer
2v55_c Q13464 ENSG00000067900 ROCK1 99.70 8.20E-23 8.10E-27 210.40 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 99.70 2.80E-23 2.80E-27 212.90 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
ITK EMT LYK
Tyrosine-protein kinase ITK/TSK (EC 2.7.10.2) (Interleukin-2-inducible T-cell kinase) (IL-2-inducible T-cell kinase) (Kinase EMT) (T-cell-specific kinase) (Tyrosine-protein kinase Lyk)
2.7.10.2 Homo sapiens
Lymphopenia,Allergic Asthma,B Cell Deficiency,Pancytopenia,Angioimmunoblastic T-Cell Lymphoma,Mixed Oligodendroglioma-Astrocytoma,Lymphoproliferative Syndrome 1,Agammaglobulinemia,Lymphoproliferative Syndrome 2,Epidermodysplasia Verruciformis 1,Cone-Rod Dystrophy 2,Disease Of Mental Health,Immunodeficiency 17,Thrombocytopenia,Hemophagocytic Lymphohistiocytosis,Lymphoproliferative Syndrome, X-Linked, 2,Agammaglobulinemia, X-Linked,Immunodeficiency, X-Linked, With Magnesium Defect, Epstein-Barr Virus Infection, And Neoplasia,Peripheral T-Cell Lymphoma,Epilepsy, Familial Temporal Lobe, 8,Coronin-1a Deficiency,Lymphoproliferative Syndrome, X-Linked, 1,Lymphoproliferative Syndrome,Asthma
4hct_a Q08881 ENSG00000113263 ITK 99.40 1.80E-17 1.90E-21 155.50 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 6.10E-18 6.20E-22 168.00 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
Rop2
Rop2
Toxoplasma gondii
3dzo_a Q06AK3 99.40 4.20E-17 4.10E-21 167.70 0 0 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 99.40 2.40E-17 2.50E-21 156.60 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
PRKCQ PRKCT
Protein kinase C theta type (EC 2.7.11.13) (nPKC-theta)
2.7.11.13 Homo sapiens
Inflammatory Bowel Disease 1,T-Cell Lymphoblastic Leukemia/Lymphoma,Crohn'S Disease,Breast Cancer,Gastrointestinal Stromal Tumor
4ra5_a Q04759 ENSG00000065675 PRKCQ 99.60 6.00E-21 6.00E-25 189.60 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
CDK5 CDKN5
Cyclin-dependent-like kinase 5 (EC 2.7.11.1) (Cell division protein kinase 5) (Serine/threonine-protein kinase PSSALRE) (Tau protein kinase II catalytic subunit) (TPKII catalytic subunit)
2.7.11.1 Homo sapiens
Cerebellar Hypoplasia,Supranuclear Palsy, Progressive, 1,Polycystic Kidney Disease,Dyslexia,Alzheimer Disease,Amyotrophic Lateral Sclerosis 1,Transient Cerebral Ischemia,Giant Axonal Neuropathy 2,Motor Neuron Disease,Neuroblastoma,Hereditary Spastic Paraplegia,Nephronophthisis,Alzheimer Disease 9,Scrapie,Parkinson Disease, Late-Onset,Lissencephaly With Cerebellar Hypoplasia,Pick Disease Of Brain,Ischemia,Developmental And Epileptic Encephalopathy 5,Disease Of Mental Health,Toxic Encephalopathy,Dementia, Lewy Body,Lissencephaly,Aneurysmal Bone Cysts,Lissencephaly 7 With Cerebellar Hypoplasia,Syndromic Intellectual Disability,Non-Syndromic Intellectual Disability,Multiple System Atrophy 1,Myasthenic Syndrome, Congenital, 19,Primary Autosomal Recessive Microcephaly,C Syndrome,Lung Cancer
4au8_b Q00535 ENSG00000164885 CDK5 99.40 3.10E-17 3.30E-21 156.40 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
pknB Rv0014c MTCY10H4.14c
Serine/threonine-protein kinase PknB (EC 2.7.11.1)
2.7.11.1 Mycobacterium tuberculosis
6i2p_a P9WI81 99.40 6.90E-18 7.30E-22 159.00 0 0 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
pknE Rv1743 MTCY28.05
Serine/threonine-protein kinase PknE (EC 2.7.11.1)
2.7.11.1 Mycobacterium tuberculosis
2h34_a P9WI77 99.40 4.90E-18 5.00E-22 165.60 0 0 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 99.40 7.50E-18 7.40E-22 166.80 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
Prkcb Pkcb Prkcb1
Protein kinase C beta type (PKC-B) (PKC-beta) (EC 2.7.11.13)
2.7.11.13 Rattus norvegicus
3pfq_a P68403 99.60 1.10E-19 1.10E-23 199.10 0 0 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 99.40 3.90E-17 4.10E-21 156.90 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
PRKAA2 AMPK AMPK2
5'-AMP-activated protein kinase catalytic subunit alpha-2 (AMPK subunit alpha-2) (EC 2.7.11.1) (Acetyl-CoA carboxylase kinase) (ACACA kinase) (EC 2.7.11.27) (Hydroxymethylglutaryl-CoA reductase kinase) (HMGCR kinase) (EC 2.7.11.31)
2.7.11.27,2.7.11.31, Homo sapiens
Hyperglycemia,Hypertrophic Cardiomyopathy,Glycogen Storage Disease,Phosphorylase Kinase Deficiency,Tuberous Sclerosis,Breast Cancer,Ischemia,Aromatase Deficiency,Peutz-Jeghers Syndrome,Body Mass Index Quantitative Trait Locus 11,Type 2 Diabetes Mellitus,Wolff-Parkinson-White Syndrome
2h6d_a P54646 ENSG00000162409 PRKAA2 99.40 3.00E-17 3.20E-21 155.60 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 99.40 3.80E-17 3.90E-21 160.70 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 99.70 4.50E-23 4.50E-27 212.60 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 99.50 2.10E-18 2.10E-22 170.30 0 0 1 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 99.40 6.20E-18 6.50E-22 162.80 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
PLK3 CNK FNK PRK
Serine/threonine-protein kinase PLK3 (EC 2.7.11.21) (Cytokine-inducible serine/threonine-protein kinase) (FGF-inducible kinase) (Polo-like kinase 3) (PLK-3) (Proliferation-related kinase)
2.7.11.21 Homo sapiens
Breast Cancer
4b6l_a Q9H4B4 ENSG00000173846 PLK3 99.40 3.90E-17 4.10E-21 155.90 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 99.50 3.80E-18 3.90E-22 169.50 0 0 1 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 99.40 5.00E-18 4.90E-22 172.60 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
CDPK1
CDPK1
Toxoplasma gondii
5t6i_a Q9BJF5 99.40 1.70E-17 1.70E-21 174.70 0 0 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 99.50 1.30E-18 1.30E-22 173.50 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
MASTL GW GWL THC2
Serine/threonine-protein kinase greatwall (GW) (GWL) (hGWL) (EC 2.7.11.1) (Microtubule-associated serine/threonine-protein kinase-like) (MAST-L)
2.7.11.1 Homo sapiens
Autosomal Thrombocytopenia With Normal Platelets,Sick Building Syndrome,Thrombocytopenia,Thrombocytopenia 2,Gray Platelet Syndrome,Ceroid Lipofuscinosis, Neuronal, 2
5loh_a Q96GX5 ENSG00000120539 MASTL 99.70 4.20E-21 4.20E-25 192.30 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
CIPK23 LKS1 PKS17 SnRK3.23 At1g30270 F12P21.6
CBL-interacting serine/threonine-protein kinase 23 (EC 2.7.11.1) (Protein LOW-K(+)-SENSITIVE 1) (SNF1-related kinase 3.23) (SOS2-like protein kinase PKS17)
2.7.11.1 Arabidopsis thaliana
4czt_d Q93VD3 99.40 1.80E-17 1.70E-21 175.50 0 0 0 0 0 0 1 0
YGR092W DBF2 SGDID:S000003324
DAPK1 DAPK
Death-associated protein kinase 1 (DAP kinase 1) (EC 2.7.11.1)
2.7.11.1 Homo sapiens
Squamous Cell Carcinoma,Childhood Acute Lymphocytic Leukemia,Lung Cancer Susceptibility 3,Adenoid Cystic Carcinoma,Cholecystitis,Alzheimer Disease,B-Cell Lymphoma,Mixed Oligodendroglioma-Astrocytoma,Transitional Cell Carcinoma,Bladder Cancer,Tuberous Sclerosis 2,Parkinson Disease, Late-Onset,Colorectal Cancer,Pediatric Lymphoma,Oligodendroglioma,Central Neurocytoma,Ischemia,Gastric Cancer,Pancreatic Ductal Adenocarcinoma,Cholangiocarcinoma,Cervical Cancer,Cervical Squamous Cell Carcinoma,Myelodysplastic Syndrome,Nasopharyngeal Carcinoma,Lung Cancer
2x0g_a P53355 ENSG00000196730 DAPK1 99.40 8.00E-18 8.10E-22 166.60 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
STK32A YANK1
Serine/threonine-protein kinase 32A (EC 2.7.11.1) (Yet another novel kinase 1)
2.7.11.1 Homo sapiens
4fr4_a Q8WU08 ENSG00000169302 STK32A 99.50 4.00E-19 4.00E-23 180.80 0 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
P0510F09.27
P0510F09.27
Oryza sativa
3sv0_a Q8LR51 99.40 1.90E-17 1.70E-21 176.20 0 0 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 99.50 1.40E-18 1.40E-22 175.30 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
CPK4 CDPK4 PF07_0072
Calcium-dependent protein kinase 4 (EC 2.7.11.1)
2.7.11.1 Plasmodium falciparum
4rgj_a Q8IBS5 99.40 1.70E-17 1.80E-21 172.70 0 0 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 1.90E-17 1.90E-21 167.20 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
TLK2
Serine/threonine-protein kinase tousled-like 2 (EC 2.7.11.1) (HsHPK) (PKU-alpha) (Tousled-like kinase 2)
2.7.11.1 Homo sapiens
Pica Disease,Mental Retardation, Autosomal Dominant 57
5o0y_a Q86UE8 ENSG00000146872 TLK2 99.40 2.20E-17 2.00E-21 180.60 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
STRADA LYK5 STRAD
STE20-related kinase adapter protein alpha (STRAD alpha) (STE20-related adapter protein) (Serologically defined breast cancer antigen NY-BR-96)
Homo sapiens
Epilepsy,Polyhydramnios,Endometrial Squamous Cell Carcinoma,Breast Cancer,Megalencephaly,Benign Epilepsy With Centrotemporal Spikes,Scheuermann Disease,Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy
2wtk_b Q7RTN6 ENSG00000266173 STRADA 99.40 2.30E-17 2.30E-21 166.00 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
aurkb-a airk2-a
Aurora kinase B-A (EC 2.7.11.1) (Aurora/IPL1-related kinase 2-A) (AIRK2-A) (XAIRK2-A) (Serine/threonine-protein kinase 12-A) (Serine/threonine-protein kinase aurora-B-A) (xAurora-B)
2.7.11.1 Xenopus laevis
4c2v_b Q6DE08 99.40 1.70E-17 1.70E-21 158.50 0 0 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
Brsk2 Kiaa4256 Sada
Serine/threonine-protein kinase BRSK2 (EC 2.7.11.1) (EC 2.7.11.26) (Brain-specific serine/threonine-protein kinase 2) (BR serine/threonine-protein kinase 2) (Serine/threonine-protein kinase SAD-A)
2.7.11.26 Mus musculus
4ynz_b Q69Z98 99.50 4.00E-19 4.00E-23 177.00 0 0 1 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
PKH2 PKH1 CAALFM_C112410CA CaO19.12690 CaO19.5224 orf19.5224
Serine/threonine-protein kinase PKH2 (EC 2.7.11.1) (PKB-activating kinase homolog 2)
2.7.11.1 Candida albicans
4c0t_a Q5A3P6 99.40 2.80E-17 2.30E-21 187.70 0 0 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 2.40E-18 2.40E-22 177.10 0 0 0 0 0 0 1 0
YGR092W DBF2 SGDID:S000003324
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 99.60 1.80E-20 1.90E-24 187.00 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
NTRK1 MTC TRK TRKA
High affinity nerve growth factor receptor (EC 2.7.10.1) (Neurotrophic tyrosine kinase receptor type 1) (TRK1-transforming tyrosine kinase protein) (Tropomyosin-related kinase A) (Tyrosine kinase receptor) (Tyrosine kinase receptor A) (Trk-A) (gp140trk) (p140-TrkA)
2.7.10.1 Homo sapiens
Spitzoid Melanoma,Megacolon,Skin Melanoma,Ganglioneuroblastoma,Follicular Adenoma,Autonomic Neuropathy,Retinitis Pigmentosa,Thyroid Gland Cancer,Adenoid Cystic Carcinoma,Peripheral Nervous System Benign Neoplasm,Autonomic Nervous System Benign Neoplasm,Leukemia, Chronic Myeloid,Thyroid Gland Anaplastic Carcinoma,Peripheral Nervous System Neoplasm,Alzheimer Disease,Chagas Disease,Tall Cell Variant Papillary Carcinoma,Amyotrophic Lateral Sclerosis 1,Diabetic Neuropathy,Differentiated Thyroid Carcinoma,Capillary Lymphangioma,Congenital Mesoblastic Nephroma,Neuropathy, Hereditary Sensory And Autonomic, Type V,Ganglioneuroma,Neuroblastoma,Multiple Endocrine Neoplasia, Type Iib,Neuroaxonal Dystrophy,Hypertrophic Pyloric Stenosis,Pyloric Stenosis,Leukemia, Acute Myeloid,Sensory Peripheral Neuropathy,Ocular Cicatricial Pemphigoid,Congenital Fibrosarcoma,Autonomic Nervous System Neoplasm,Multiple Mucosal Neuroma,Uterine Corpus Sarcoma,Benign Struma Ovarii,Malignant Giant Cell Tumor Of The Tendon Sheath,Thyroid Carcinoma,Small Intestinal Sarcoma,Uterus Leiomyosarcoma,Ntrk1 Congenital Insensitivity To Pain With Anhidrosis,Femoral Cancer,Ovarian Cancer,Neuropathy,Neuropathy, Hereditary Sensory And Autonomic, Type Iii,Charcot-Marie-Tooth Disease,Cortical Senile Cataract,Breast Cancer,Adrenal Neuroblastoma,Colorectal Cancer,Peripheral Nervous System Disease,Squamous Blepharitis,Sweat Gland Disease,Papillary Carcinoma,Premature Menopause,Oligodendroglioma,Angiokeratoma Circumscriptum,Pheochromocytoma,Multiple Endocrine Neoplasia, Type Iia,Tooth Disease,Neurogenic Arthropathy,Anhidrosis,Mesenchymal Cell Neoplasm,Cone-Rod Dystrophy 2,Prostate Cancer,Disease Of Mental Health,Mastocytosis,Pediatric Fibrosarcoma,Olfactory Neuroblastoma,Thyroid Gland Follicular Carcinoma,Thyroid Gland Medullary Carcinoma,Hereditary Sensory Neuropathy,Spinal Muscular Atrophy, Distal, Autosomal Recessive, 2,Trigeminal Neuralgia,Hirschsprung Disease 1,Attention Deficit-Hyperactivity Disorder,Neuropathy, Hereditary Sensory And Autonomic, Type Viii,Neuropathy, Hereditary Sensory And Autonomic, Type Iia,Glucocorticoid Deficiency 1,Thyroid Carcinoma, Familial Medullary,Medulloblastoma,Insensitivity To Pain, Congenital, With Anhidrosis,Pancreatic Cancer
5jfw_a P04629 ENSG00000198400 NTRK1 99.40 3.40E-17 3.50E-21 158.10 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 99.40 3.00E-17 3.10E-21 156.70 0 0 1 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 99.40 2.60E-17 2.70E-21 157.00 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
PRKACA
cAMP-dependent protein kinase catalytic subunit alpha (PKA C-alpha) (EC 2.7.11.11)
2.7.11.11 Bos taurus
2uzv_a P00517 99.60 5.70E-21 5.80E-25 190.20 0 0 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 9.20E-18 9.20E-22 169.10 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 99.40 1.30E-17 1.30E-21 159.80 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
RPS6KA5 MSK1
Ribosomal protein S6 kinase alpha-5 (S6K-alpha-5) (EC 2.7.11.1) (90 kDa ribosomal protein S6 kinase 5) (Nuclear mitogen- and stress-activated protein kinase 1) (RSK-like protein kinase) (RSKL)
2.7.11.1 Homo sapiens
Septic Myocarditis,Coffin-Lowry Syndrome
3kn5_b O75582 ENSG00000100784 RPS6KA5 99.40 2.40E-17 2.50E-21 162.10 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
ROCK2 KIAA0619
Rho-associated protein kinase 2 (EC 2.7.11.1) (Rho kinase 2) (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 Homo sapiens
Coronary Artery Vasospasm,Dextrocardia,Ureteral Obstruction,Breast Cancer,Tongue Squamous Cell Carcinoma,Hypertension, Essential
4wot_b O75116 ENSG00000134318 ROCK2 99.70 6.50E-22 6.40E-26 202.90 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 3.50E-17 3.50E-21 164.60 0 0 0 0 0 1 0 0
YGR092W DBF2 SGDID:S000003324
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 7.60E-18 7.80E-22 167.80 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 6.70E-18 6.70E-22 171.60 0 0 0 0 0 0 1 0
YGR092W DBF2 SGDID:S000003324
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 99.40 2.50E-17 2.60E-21 157.70 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
ROP8
ROP8
Toxoplasma gondii
3byv_a O15693 99.40 1.50E-17 1.50E-21 167.90 0 0 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
PDPK1 PDK1
3-phosphoinositide-dependent protein kinase 1 (hPDK1) (EC 2.7.11.1)
2.7.11.1 Homo sapiens
Endometrial Cancer,Noonan Syndrome 1,Esophageal Adenosquamous Carcinoma,Prostate Cancer,Tuberous Sclerosis 1,Lung Cancer
1h1w_a O15530 ENSG00000140992 PDPK1 99.50 2.50E-18 2.60E-22 165.50 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
AURKA AIK AIRK1 ARK1 AURA AYK1 BTAK IAK1 STK15 STK6
Aurora kinase A (EC 2.7.11.1) (Aurora 2) (Aurora/IPL1-related kinase 1) (ARK-1) (Aurora-related kinase 1) (hARK1) (Breast tumor-amplified kinase) (Serine/threonine-protein kinase 15) (Serine/threonine-protein kinase 6) (Serine/threonine-protein kinase aurora-A)
2.7.11.1 Homo sapiens
Endometrial Cancer,Melanoma,Plasma Cell Neoplasm,Uterine Corpus Cancer,Atypical Teratoid Rhabdoid Tumor,Neuroblastoma,Childhood Malignant Schwannoma,Adult Malignant Schwannoma,Bladder Cancer,Laryngeal Squamous Cell Carcinoma,Tetraploidy,Ovarian Cancer,Prostate Neuroendocrine Neoplasm,Breast Cancer,Colorectal Cancer,Endometrial Serous Adenocarcinoma,Hepatocellular Carcinoma,Rhabdomyosarcoma,Gastric Cancer,Prostate Cancer,Cervical Cancer,Lynch Syndrome,Esophageal Cancer,Donohue Syndrome,Colorectal Adenocarcinoma,Myeloma, Multiple,Medulloblastoma,Primary Autosomal Recessive Microcephaly,Lung Cancer,Pancreatic Cancer
3h10_a O14965 ENSG00000087586 AURKA 99.40 5.80E-18 6.10E-22 160.00 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 2.30E-17 2.30E-21 165.50 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
SGK1 SGK
Serine/threonine-protein kinase Sgk1 (EC 2.7.11.1) (Serum/glucocorticoid-regulated kinase 1)
2.7.11.1 Homo sapiens
Plasma Cell Neoplasm,Pseudohypoaldosteronism,Cystic Fibrosis,Gastric Cancer,Disease Of Mental Health,Liddle Syndrome 1,Body Mass Index Quantitative Trait Locus 11,Pseudohypoaldosteronism, Type I, Autosomal Dominant,Tuberous Sclerosis 1,Hypertension, Essential,Rett Syndrome,Myeloma, Multiple
2r5t_a O00141 ENSG00000118515 SGK1 99.60 3.20E-20 3.20E-24 187.70 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
PTSG_10090
PTSG_10090
2.7.11.17 Salpingoeca rosetta
5ig1_b F2UPG5 99.40 2.50E-17 2.50E-21 164.40 0 0 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
pknB MRA_0016
pknB MRA_0016
2.7.11.1 Mycobacterium tuberculosis
3ork_a A5TY84 99.40 4.00E-17 4.10E-21 158.20 0 0 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
SA1063
SA1063
Staphylococcus aureus
4eqm_b A0A0H3JME9 99.40 1.10E-17 1.10E-21 160.30 0 0 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
GRK1 RHOK
Rhodopsin kinase GRK1 (RK) (EC 2.7.11.14) (G protein-coupled receptor kinase 1)
2.7.11.14 Bos taurus
3c4z_a P28327 99.40 1.60E-17 1.50E-21 179.00 0 0 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
CDK7 CAK CAK1 CDKN7 MO15 STK1
Cyclin-dependent kinase 7 (EC 2.7.11.22) (EC 2.7.11.23) (39 kDa protein kinase) (p39 Mo15) (CDK-activating kinase 1) (Cell division protein kinase 7) (Serine/threonine-protein kinase 1) (TFIIH basal transcription factor complex kinase subunit)
2.7.11.22,2.7.11.23, Homo sapiens
Myofibrillar Myopathy,Cockayne Syndrome,Breast Cancer,Xeroderma Pigmentosum, Complementation Group D,Xeroderma Pigmentosum, Variant Type,Xeroderma Pigmentosum, Complementation Group B
1ua2_b P50613 ENSG00000134058 CDK7 99.40 8.20E-18 8.40E-22 166.60 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 2.70E-17 2.70E-21 162.20 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
GRK6 GPRK6
G protein-coupled receptor kinase 6 (EC 2.7.11.16) (G protein-coupled receptor kinase GRK6)
2.7.11.16 Homo sapiens
Whim Syndrome
3nyn_b P43250 ENSG00000198055 GRK6 99.60 2.00E-19 1.80E-23 195.90 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
PRKCI DXS1179E
Protein kinase C iota type (EC 2.7.11.13) (Atypical protein kinase C-lambda/iota) (PRKC-lambda/iota) (aPKC-lambda/iota) (nPKC-iota)
2.7.11.13 Homo sapiens
Glioblastoma,Lung Squamous Cell Carcinoma,Lung Cancer
3a8x_a P41743 ENSG00000163558 PRKCI 99.60 7.90E-20 8.10E-24 181.40 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 99.40 5.40E-18 5.50E-22 167.40 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 99.40 1.00E-17 1.00E-21 172.00 0 0 1 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 1.60E-17 1.60E-21 165.00 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
GRK5 GPRK5
G protein-coupled receptor kinase 5 (EC 2.7.11.16) (G protein-coupled receptor kinase GRK5)
2.7.11.16 Homo sapiens
Systolic Heart Failure,Palmoplantar Keratoderma And Congenital Alopecia 2,Asthma
4tnd_a P34947 ENSG00000198873 GRK5 99.60 2.00E-19 1.80E-23 197.10 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
AKT1 PKB RAC
RAC-alpha serine/threonine-protein kinase (EC 2.7.11.1) (Protein kinase B) (PKB) (Protein kinase B alpha) (PKB alpha) (Proto-oncogene c-Akt) (RAC-PK-alpha)
2.7.11.1 Homo sapiens
Adult Hepatocellular Carcinoma,Breast Papillomatosis,Esophageal Disease,Pancreatic Adenocarcinoma,Muscular Disease,Skin Melanoma,Liver Disease,Mitral Valve Disease,Heart Disease,Neurofibromatosis, Type Ii,Endometrial Cancer,Bile Duct Disease,Spinal Chordoma,Hepatopulmonary Syndrome,Squamous Cell Carcinoma,Pfeiffer Syndrome,Glucose Metabolism Disease,Childhood T-Cell Acute Lymphoblastic Leukemia,Hyperglycemia,Retinitis Pigmentosa,Thyroid Gland Cancer,Hair Disease,Macroglobulinemia,Lung Cancer Susceptibility 3,Kagami-Ogata Syndrome,Adenoid Cystic Carcinoma,Non-Alcoholic Fatty Liver Disease,Chordoma,Cowden Syndrome,Polycystic Kidney Disease,Microvascular Complications Of Diabetes 5,Suppression Of Tumorigenicity 12,Melanoma,Connective Tissue Disease,Ocular Hypertension,Leukemia, Chronic Myeloid,Overnutrition,Inherited Metabolic Disorder,Thyroid Gland Anaplastic Carcinoma,Diabetes Mellitus,Adenoma,Spherocytosis, Type 5,Cowden Syndrome 1,Breast Juvenile Papillomatosis,Lipid Storage Disease,Peripheral Nervous System Neoplasm,Uterine Corpus Cancer,Connective Tissue Cancer,Bone Sarcoma,Hypertrophic Cardiomyopathy,Placental Choriocarcinoma,Leukocyte Disease,Clear Cell Renal Cell Carcinoma,Hyperostosis,Alzheimer Disease,Hepatoblastoma,Rasopathy,Nasopharyngeal Disease,Myocardial Infarction,Major Depressive Disorder,Bile Duct Cancer,Intestinal Benign Neoplasm,Stroke, Ischemic,Teeth Hard Tissue Disease,Amyotrophic Lateral Sclerosis 1,Malignant Ovarian Surface Epithelial-Stromal Neoplasm,Ovary Epithelial Cancer,T-Cell Lymphoblastic Leukemia/Lymphoma,Ocular Cancer,Amelogenesis Imperfecta,Retinal Cancer,Blood Platelet Disease,Biliary Tract Disease,Congenital Lipomatous Overgrowth, Vascular Malformations, And Epidermal Nevi,Infratentorial Cancer,Leptin Deficiency Or Dysfunction,Lymphatic System Disease,Neurofibromatosis, Type I,Insulin-Like Growth Factor I,Neuroblastoma,Colonic Benign Neoplasm,Subependymal Glioma,Blood Coagulation Disease,Benign Ependymoma,Pilocytic Astrocytoma,Diffuse Astrocytoma,Childhood Leukemia,Bile Duct Adenocarcinoma,Hemangioma Of Lung,Nevus, Epidermal,Distal Muscular Dystrophy With Anterior Tibial Onset,Retinal Vascular Disease,Psychotic Disorder,Leukemia, Acute Myeloid,Noonan Syndrome 1,Bone Marrow Cancer,Leber Plus Disease,Hemangioma,Leukemia, Acute Lymphoblastic,Cataract,Combined Immunodeficiency,Liver Cirrhosis,Pancreas Disease,Papilloma,Cardiovascular System Disease,Autonomic Nervous System Neoplasm,Kidney Cancer,Pleural Cancer,Basal Cell Nevus Syndrome,Cowden Syndrome 6,Bladder Cancer,Focal Segmental Glomerulosclerosis,Epithelial-Myoepithelial Carcinoma,Thymus Gland Disease,Brain Cancer,Colonic Disease,Lung Adenoma,Lung Oat Cell Carcinoma,Endometrial Adenocarcinoma,Oropharynx Cancer,Cervix Carcinoma,Ulcerative Colitis,Nervous System Disease,Osteoporosis,Anal Squamous Cell Carcinoma,Ovarian Cancer,Adenocarcinoma,Tuberous Sclerosis 2,In Situ Carcinoma,Tuberous Sclerosis,T-Cell Acute Lymphoblastic Leukemia,Eye Disease,Acute Megakaryocytic Leukemia,Breast Carcinoma In Situ,Breast Cancer,Glioblastoma,Squamous Cell Carcinoma, Head And Neck,Malignant Astrocytoma,Gliosarcoma,Parkinson Disease, Late-Onset,Colorectal Cancer,Peripheral Nervous System Disease,Nervous System Cancer,Ovarian Serous Cystadenocarcinoma,Cystadenocarcinoma,Serous Cystadenocarcinoma,Gallbladder Cancer,Hepatocellular Carcinoma,Premature Menopause,Combined Hepatocellular Carcinoma And Cholangiocarcinoma,Skin Papilloma,Partial Third-Nerve Palsy,Neurilemmoma,Rhabdomyosarcoma,Ischemia,Tongue Disease,Chronic Granulomatous Disease,Thymoma,Thymus Cancer,Ovarian Disease,Noonan Syndrome With Multiple Lentigines,Polycystic Kidney Disease 1 With Or Without Polycystic Liver Disease,Teratoma,Bipolar Disorder,Macular Degeneration, Age-Related, 1,Immunodeficiency 14,Sarcoma,Bone Osteosarcoma,Skin Carcinoma,Gastric Cancer,Breast Adenocarcinoma,Cone-Rod Dystrophy 2,Prostate Cancer,Disease Of Mental Health,Pancreatic Ductal Adenocarcinoma,Cholangiocarcinoma,Proteus Syndrome,Cervical Cancer,Toxic Encephalopathy,Ovarian Cystadenocarcinoma,Body Mass Index Quantitative Trait Locus 11,Penile Disease,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Central Nervous System Cancer,Pulmonary Fibrosis, Idiopathic,Congenital Myasthenic Syndrome,Retinitis Pigmentosa 47,Respiratory System Disease,Integumentary System Disease,Skin Disease,Cervical Adenocarcinoma,Ovary Adenocarcinoma,Gastric Adenocarcinoma,Type 2 Diabetes Mellitus,Plasmacytoma,Cervical Squamous Cell Carcinoma,Lynch Syndrome,Hidradenoma,Lung Squamous Cell Carcinoma,Fragile X Syndrome,Thyroid Gland Follicular Carcinoma,Schizophrenia,Sensory System Disease,Bladder Urothelial Carcinoma,Lymphoma, Non-Hodgkin, Familial,Skeletal Muscle Cancer,Muscle Cancer,Small Cell Cancer Of The Lung,Immunodeficiency 36,Hypotrichosis 1,Exanthem,Esophageal Cancer,Severe Congenital Neutropenia,Respiratory System Benign Neoplasm,Reproductive Organ Benign Neoplasm,Gastrointestinal System Benign Neoplasm,Immune Deficiency Disease,Myelodysplastic Syndrome,Meningioma, Radiation-Induced,Wiskott-Aldrich Syndrome,X-Linked Monogenic Disease,Autosomal Genetic Disease,Diffuse Large B-Cell Lymphoma,Ewing Sarcoma,Mantle Cell Lymphoma,Peripheral T-Cell Lymphoma,Tuberous Sclerosis 1,Hashimoto Thyroiditis,Gastrointestinal Stromal Tumor,Diabetic Encephalopathy,Tongue Squamous Cell Carcinoma,Oral Squamous Cell Carcinoma,Huntington Disease,Renal Cell Carcinoma, Nonpapillary,Nasopharyngeal Carcinoma,Hypertension, Essential,Meningioma, Familial,Pre-Malignant Neoplasm,Lymphatic System Cancer,Ductal Carcinoma In Situ,Estrogen-Receptor Positive Breast Cancer,Cell Type Benign Neoplasm,Cardiovascular Organ Benign Neoplasm,Uterine Benign Neoplasm,Acquired Metabolic Disease,Kaposi Sarcoma,Colitis,Klippel-Trenaunay-Weber Syndrome,Gallbladder Disease,Leukemia, Chronic Lymphocytic,Amelogenesis Imperfecta, Type Ig,Systemic Lupus Erythematosus,Pelizaeus-Merzbacher Disease,Rett Syndrome,Myeloma, Multiple,Medulloblastoma,Spinal Disease,Autism,Melanoma, Cutaneous Malignant 1,Melanoma, Uveal,Lymphoproliferative Syndrome,Lung Cancer,Palmoplantar Keratoderma, Bothnian Type,Oculoectodermal Syndrome,Osteogenic Sarcoma,Pancreatic Cancer
4gv1_a P31749 ENSG00000142208 AKT1 99.70 1.20E-21 1.20E-25 195.60 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
HRR25 YPL204W
Casein kinase I homolog HRR25 (EC 2.7.11.1)
2.7.11.1 Saccharomyces cerevisiae
5cyz_a P29295 99.40 1.00E-17 1.00E-21 170.20 0 0 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 99.90 2.10E-28 1.90E-32 248.90 0 0 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
MARK3 CTAK1 EMK2
MAP/microtubule affinity-regulating kinase 3 (EC 2.7.11.1) (C-TAK1) (cTAK1) (Cdc25C-associated protein kinase 1) (ELKL motif kinase 2) (EMK-2) (Protein kinase STK10) (Ser/Thr protein kinase PAR-1) (Par-1a) (Serine/threonine-protein kinase p78)
2.7.11.1 Homo sapiens
Focal Epithelial Hyperplasia,Osteoporosis,Peutz-Jeghers Syndrome,Gaucher Disease, Type Iii,Visual Impairment And Progressive Phthisis Bulbi
2qnj_b P27448 ENSG00000075413 MARK3 99.40 3.40E-17 3.50E-21 160.90 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
PRKACA
cAMP-dependent protein kinase catalytic subunit alpha (PKA C-alpha) (EC 2.7.11.11)
2.7.11.11 Cricetulus griseus
5n3j_a P25321 99.60 8.10E-21 8.20E-25 190.30 0 0 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 99.50 1.40E-18 1.20E-22 194.00 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
PRKCH PKCL PRKCL
Protein kinase C eta type (EC 2.7.11.13) (PKC-L) (nPKC-eta)
2.7.11.13 Homo sapiens
Myofibrillar Myopathy,Amphetamine Abuse,Stroke, Ischemic,Glioblastoma
3txo_a P24723 ENSG00000027075 PRKCH 99.60 2.30E-20 2.30E-24 186.60 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
JAK1 JAK1A JAK1B
Tyrosine-protein kinase JAK1 (EC 2.7.10.2) (Janus kinase 1) (JAK-1)
2.7.10.2 Homo sapiens
Psoriasis,Breast Implant-Associated Anaplastic Large Cell Lymphoma,Endometrial Cancer,Severe Combined Immunodeficiency,Hepatitis C,Covid-19,Blood Platelet Disease,Hepatitis,Leukemia,Blood Coagulation Disease,Wernicke Encephalopathy,Leukemia, Acute Myeloid,Sting-Associated Vasculopathy With Onset In Infancy,Bone Marrow Cancer,Leukemia, Acute Lymphoblastic,Combined Immunodeficiency,Polycythemia,Autosomal Recessive Mendelian Susceptibility To Mycobacterial Diseases Due To Partial Jak1 Deficiency,Crisponi/Cold-Induced Sweating Syndrome 1,Colonic Disease,Acute Megakaryoblastic Leukemia In Down Syndrome,Herpes Zoster,Autoimmune Lymphoproliferative Syndrome,T-Cell Prolymphocytic Leukemia,Mixed Lacrimal Gland Cancer,Prolymphocytic Leukemia,Nasopharyngitis,Ovarian Cancer,T-Cell Acute Lymphoblastic Leukemia,Acute Megakaryocytic Leukemia,Breast Cancer,Colorectal Cancer,Hepatocellular Carcinoma,Jak3-Deficient Severe Combined Immunodeficiency,Fibrosarcoma,Prostate Cancer,Chilblain Lupus 1,Severe Combined Immunodeficiency, X-Linked,Mouth Disease,Immunodeficiency 27b,Immunodeficiency 35,Aicardi-Goutieres Syndrome,Down Syndrome,Acute Promyelocytic Leukemia,Lymphoblastic Leukemia, Acute, With Lymphomatous Features,Leukemia, Acute, X-Linked,Alopecia Universalis Congenita,Autoinflammation, Immune Dysregulation, And Eosinophilia,Systemic Lupus Erythematosus,Myelofibrosis,Lymphoproliferative Syndrome,Immunodeficiency 27a,Pancreatic Cancer,Polycythemia Vera
3eyh_a P23458 ENSG00000162434 JAK1 99.40 2.30E-17 2.40E-21 156.50 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 99.50 7.50E-19 7.70E-23 173.40 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 6.40E-18 6.50E-22 168.10 0 0 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 2.60E-17 2.60E-21 164.50 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
PRKACA PKACA
cAMP-dependent protein kinase catalytic subunit alpha (PKA C-alpha) (EC 2.7.11.11)
2.7.11.11 Homo sapiens
Mixed Fibrolamellar Hepatocellular Carcinoma,Fibrolamellar Carcinoma,Cardioacrofacial Dysplasia 1,Dilated Cardiomyopathy,Acth-Independent Cushing Syndrome,Osteoporosis,Breast Cancer,Pigmented Nodular Adrenocortical Disease, Primary, 4,Primary Pigmented Nodular Adrenocortical Disease
3ama_a P17612 ENSG00000072062 PRKACA 99.70 3.60E-21 3.60E-25 192.90 1 1 0 0 0 0 0 0
YGR092W DBF2 SGDID:S000003324
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 99.40 2.60E-17 2.60E-21 167.00 1 1 0 0 0 0 0 0

Weizmann Institute of Science | Maya Schuldiner Lab