Allelic Variants

There are no related allelic variants
Related diseases of KIF 2IVUA_ZD6 (PDB code: 2IVU, chain A)
Number of involved diseases in the family 121
Number of RET related diseases 9
All kinase in this family  RET
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
Prostate cancerEGFR, ERBB2, FGFR1, FGFR2,
MAP2K1, PDGFRA, PDGFRB,
PDPK1
156Link
n/aMeaslesFYN, IRAK4, JAK2, JAK3,
MAP3K7, PRKCQ, TYK2
12Link
LeukemiaABL1, ABL2, JAK2, KIT,
MAP2K1, PDGFRB
29Link
MelanomaEGFR, FGFR1, MAP2K1, MET,
PDGFRA, PDGFRB
155Link
n/aEpstein-Barr virus infectionFGR, JAK3, MAP3K7, SYK, TYK212Link
n/aTuberculosisIRAK4, JAK2, SRC, SYK136Link
NeuroblastomaALK, NTRK1, NTRK2, NTRK38Link
n/aInfluenza AIRAK4, JAK2, MAP2K1, TYK212Link
n/aEpithelial cell signaling in Helicobacter pylori infectionCSK, EGFR, MET, SRC267Link
n/aToxoplasmosisIRAK4, JAK2, MAP3K7, TYK27Link
Gastric cancerEGFR, ERBB2, FGFR2, MET149Link
n/aImmunodeficienciesJAK3, LCK, ZAP7021Link
n/aLeishmaniasisIRAK4, JAK2, MAP3K77Link
n/aBladder cancerEGFR, ERBB2, FGFR3149Link
n/aHerpes simplex infectionJAK2, MAP3K7, TYK23Link
n/aGliomaEGFR, PDGFRA, PDGFRB149Link
n/aCervical cancerEGFR, ERBB2, FGFR3149Link
Lung cancerALK, EGFR, PTK2149Link
n/aViral myocarditisABL1, ABL2, FYN25Link
n/aChoriocarcinomaCSF1R, EGFR, ERBB2159Link
Gastrointestinal stromal tumorKIT, PDGFRA14Link
Colon cancerAURKA, SRC137Link
n/aCholangiocarcinomaERBB2, MET25Link
n/aSalmonella infectionPKN1, PKN21Link
Pfeiffer syndromeFGFR1, FGFR233Link
SCIDJAK3, LCK21Link
n/aPrion diseasesFYN, MAP2K112Link
n/aPathogenic Escherichia coli infectionABL1, FYN25Link
n/aShigellosisABL1, SRC136Link
n/aType I diabetes mellitusERBB3, PRKCQ6Link
n/aMyeloproliferative disorderJAK2, PDGFRB10Link
LADD syndromeFGFR2, FGFR35Link
n/aThyroid cancerNTRK1, RET11Link
Adenocarcinoma of lungEGFR, ERBB2149Link
Jackson-Weiss syndromeFGFR1, FGFR233Link
n/aMedullary thyroid carcinomaNTRK1, RET11Link
n/aHepatitis CEGFR, TYK2149Link
Crouzon syndromeFGFR2, FGFR35Link
n/aAlcoholismMAP2K1, NTRK29Link
Beare-Stevenson cutis gyrata syndromeFGFR25Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR25Link
Apert syndromeFGFR25Link
Kallmann syndromeFGFR133Link
n/aSaethre-Chotzen syndromeFGFR25Link
CraniosynostosisFGFR25Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR25Link
Bent bone dysplasia syndromeFGFR25Link
Breast cancerERBB225Link
TrigonocephalyFGFR133Link
n/aAgammaglobulinemia and isolated hormone deficiencyBTK9Link
n/aLeukoencephalopathy, diffuse hereditary, with spheroidsCSF1R18Link
n/aSpondylometaepiphyseal dysplasiaDDR25Link
AgammaglobulinemiaBTK9Link
n/aPituitary DwarfismBTK9Link
n/aDopamine receptor D2ANKK11Link
n/aMaturity onset diabetes of the youngBLK12Link
n/aAgammaglobulinemiasBTK9Link
n/aOral cancerEGFR149Link
n/aEsophageal cancerEGFR149Link
n/aLethal congenital contractural syndromeERBB36Link
Hypogonadotropic hypogonadismFGFR133Link
Osteoglophonic dysplasiaFGFR133Link
GlioblastomaERBB225Link
ScaphocephalyFGFR25Link
n/aLaryngeal cancerEGFR149Link
n/aPancreatic cancerERBB225Link
Endometrial CancerERBB225Link
Ovarian cancerERBB225Link
n/aNevusFGFR34Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR25Link
n/aHypereosinophilic syndromePDGFRA8Link
n/aAmoebiasisPTK23Link
n/aRenal agenesis and Renal adysplasiaRET10Link
Hirschsprung diseaseRET10Link
n/aObesityNTRK22Link
n/aInsensitivity to painNTRK12Link
Retinitis pigmentosaMERTK7Link
Renal cell carcinomaMET10Link
n/aMalariaMET10Link
Hepatocellular carcinomaMET10Link
n/aAutism suseptibilityMET10Link
n/aCongenital central hypoventilation syndromeRET10Link
Central hypoventilation syndromeRET10Link
n/aBasal cell carcinomaSTK366Link
n/aTransient erythroblastopenia of childhoodTEC4Link
n/aTyrosine kinase 2 deficiencyTYK21Link
Selective T-cell defectZAP701Link
Mental retardationRPS6KA31Link
n/aCoffin-Lowry syndromeRPS6KA31Link
Multiple endocrine neoplasiaRET10Link
PheochromocytomaRET10Link
Renal agenesisRET10Link
n/aNon-syndromic X-linked mental retardationRPS6KA31Link
n/aPopliteal pterygium syndromeRIPK41Link
Cardiofaciocutaneous syndromeMAP2K18Link
n/aNoonan syndrome and related disordersMAP2K18Link
n/aSpermatocytic seminomaFGFR34Link
n/aThanatophoric dysplasiaFGFR34Link
n/aCancer progression/metastasisFGFR42Link
n/aPertussisIRAK46Link
n/aMuenke syndromeFGFR34Link
n/aHypochondroplasiaFGFR34Link
n/aMultiple myelomaFGFR34Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR34Link
n/aCATSHL syndromeFGFR34Link
Colorectal cancerFGFR34Link
n/aAchondroplasiaFGFR34Link
n/aChagas diseaseIRAK46Link
n/aInvasive pneumococcal diseaseIRAK46Link
n/aGerm cell tumorsKIT13Link
Mast cell leukemiaKIT13Link
Mastocytosis with associated hematologic disorderKIT13Link
n/aParkinson diseaseLRRK22Link
n/aLewy body dementiaLRRK22Link
PiebaldismKIT13Link
ThrombocythemiaJAK22Link
IRAK4 deficiencyIRAK46Link
Lymphoproliferative syndromeITK4Link
Polycythemia veraJAK22Link
MyelofibrosisJAK22Link
n/aBudd-Chiari syndromeJAK22Link