Allelic Variants

There are no related allelic variants
Related diseases of KIF 1YVJA_4ST (PDB code: 1YVJ, chain A)
Number of involved diseases in the family 126
Number of TEC related diseases 1
All kinase in this family  TEC
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
Prostate cancerAKT2, AKT3, CDK2, EGFR,
ERBB2, FGFR1, FGFR2, GSK3B,
MAP2K1, PDGFRA, PDGFRB,
PDPK1, RAF1
44Link
LeukemiaABL1, ABL2, AKT2, AKT3,
JAK2, KIT, MAP2K1, PDGFRB,
RAF1, RPS6KB1
16Link
n/aEpstein-Barr virus infectionAKT2, AKT3, CDC2, CDK2, FGR,
GSK3B, JAK1, JAK3, MAP3K7,
SYK
16Link
n/aMeaslesAKT2, AKT3, CDK2, FYN,
GSK3B, JAK1, JAK2, JAK3,
MAP3K7, PRKCQ
16Link
n/aInfluenza AAKT2, AKT3, GSK3B, JAK1,
JAK2, MAP2K1, PRKCA, PRKCB,
RAF1
59Link
MelanomaAKT2, AKT3, EGFR, FGFR1,
MAP2K1, MET, PDGFRA, PDGFRB,
RAF1
41Link
n/aTuberculosisAKT2, AKT3, JAK1, JAK2,
RAF1, RIPK2, SRC, SYK
20Link
n/aHepatitis CAKT2, AKT3, EGFR, GSK3B,
JAK1, RAF1
39Link
Lung cancerAKT2, AKT3, ALK, CDK2, EGFR,
ROS1
42Link
n/aHerpes simplex infectionCDC2, CDK2, JAK1, JAK2,
MAP3K7
14Link
n/aToxoplasmosisAKT2, AKT3, JAK1, JAK2,
MAP3K7
10Link
n/aEpithelial cell signaling in Helicobacter pylori infectionCSK, EGFR, MET, SRC40Link
n/aLeishmaniasisJAK1, JAK2, MAP3K7, PRKCB13Link
n/aAlcoholismCAMKK2, MAP2K1, NTRK2, RAF112Link
Gastric cancerEGFR, ERBB2, FGFR2, MET38Link
n/aShigellosisABL1, RIPK2, SRC19Link
n/aPathogenic Escherichia coli infectionABL1, FYN, PRKCA60Link
n/aChoriocarcinomaCSF1R, EGFR, ERBB239Link
n/aCervical cancerEGFR, ERBB2, FGFR337Link
n/aGliomaEGFR, PDGFRA, PDGFRB40Link
NeuroblastomaALK, NTRK2, NTRK310Link
n/aViral myocarditisABL1, ABL2, FYN13Link
n/aBladder cancerEGFR, ERBB2, FGFR337Link
n/aImmunodeficienciesJAK3, ZAP7014Link
Gastrointestinal stromal tumorKIT, PDGFRA12Link
Pfeiffer syndromeFGFR1, FGFR29Link
Adenocarcinoma of lungEGFR, ERBB237Link
n/aPrion diseasesFYN, MAP2K111Link
n/aVibrio cholerae infectionPRKCA, PRKCB54Link
Jackson-Weiss syndromeFGFR1, FGFR29Link
Crouzon syndromeFGFR2, FGFR38Link
Diabetes mellitusAKT2, INSR8Link
n/aChagas diseaseAKT2, AKT37Link
Ovarian cancerAKT2, ERBB27Link
LADD syndromeFGFR2, FGFR38Link
Colon cancerAURKA, SRC18Link
n/aSalmonella infectionPKN1, PKN211Link
n/aAmoebiasisPRKCA, PRKCB54Link
n/aCholangiocarcinomaERBB2, MET8Link
n/aMyeloproliferative disorderJAK2, PDGFRB12Link
n/aAfrican trypanosomiasisPRKCA, PRKCB54Link
TrigonocephalyFGFR19Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR28Link
Kallmann syndromeFGFR19Link
Osteoglophonic dysplasiaFGFR19Link
CraniosynostosisFGFR28Link
Bent bone dysplasia syndromeFGFR28Link
Beare-Stevenson cutis gyrata syndromeFGFR28Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR28Link
Apert syndromeFGFR28Link
n/aOral cancerEGFR37Link
Hypogonadotropic hypogonadismFGFR19Link
n/aPituitary DwarfismBTK5Link
AgammaglobulinemiaBTK5Link
n/aAgammaglobulinemiasBTK5Link
n/aMaturity onset diabetes of the youngBLK8Link
n/aFamilial partial lipodystrophyAKT27Link
Hypoinsulinemic hypoglycemiaAKT27Link
n/aAgammaglobulinemia and isolated hormone deficiencyBTK5Link
n/aLeukoencephalopathy, diffuse hereditary, with spheroidsCSF1R10Link
Breast cancerERBB22Link
GlioblastomaERBB22Link
Endometrial CancerERBB22Link
n/aPancreatic cancerERBB22Link
n/aSaethre-Chotzen syndromeFGFR28Link
n/aEsophageal cancerEGFR37Link
n/aLaryngeal cancerEGFR37Link
n/aCATSHL syndromeFGFR37Link
ScaphocephalyFGFR28Link
n/aHypereosinophilic syndromePDGFRA10Link
n/aPituitary tumorPRKCA54Link
n/aCerebral infarctionPRKCH11Link
LEOPARD syndromeRAF12Link
n/aType I diabetes mellitusPRKCQ8Link
n/aObesityNTRK29Link
n/aMyasthenic syndromeMUSK5Link
Renal cell carcinomaMET8Link
n/aMalariaMET8Link
n/aAutism suseptibilityMET8Link
n/aCongenital myasthenic syndromeMUSK5Link
Hepatocellular carcinomaMET8Link
Noonan syndromeRAF12Link
n/aThyroid cancerRET9Link
n/aPopliteal pterygium syndromeRIPK41Link
n/aTransient erythroblastopenia of childhoodTEC2Link
Venous malformationsTEK32Link
Selective T-cell defectZAP7010Link
n/aRheumatoid arthritisTEK32Link
Renal agenesisRET9Link
PheochromocytomaRET9Link
Hirschsprung diseaseRET9Link
n/aRenal agenesis and Renal adysplasiaRET9Link
n/aCongenital central hypoventilation syndromeRET9Link
Central hypoventilation syndromeRET9Link
Multiple endocrine neoplasiaRET9Link
n/aMedullary thyroid carcinomaRET9Link
Cardiofaciocutaneous syndromeMAP2K14Link
n/aNoonan syndrome and related disordersMAP2K14Link
n/aSpermatocytic seminomaFGFR37Link
n/aThanatophoric dysplasiaFGFR37Link
n/aCancer progression/metastasisFGFR43Link
n/aOguchi diseaseGRK14Link
n/aCongenital stationary night blindnessGRK14Link
n/aNevusFGFR37Link
n/aMuenke syndromeFGFR37Link
n/aMultiple myelomaFGFR37Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR28Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR37Link
n/aAchondroplasiaFGFR37Link
n/aHypochondroplasiaFGFR37Link
Colorectal cancerFGFR37Link
n/aBasal cell carcinomaGSK3B10Link
n/aEndocrine-cerebroosteodysplasiaICK2Link
SCIDJAK313Link
PiebaldismKIT12Link
n/aGerm cell tumorsKIT12Link
Mastocytosis with associated hematologic disorderKIT12Link
Mast cell leukemiaKIT12Link
ThrombocythemiaJAK210Link
MyelofibrosisJAK210Link
Rabson-Mendenhall syndromeINSR5Link
n/aLeprechaunismINSR5Link
Hyperinsulinemic hypoglycemiaINSR5Link
Lymphoproliferative syndromeITK6Link
n/aBudd-Chiari syndromeJAK210Link
Polycythemia veraJAK210Link