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 FGFR3 related diseases 14
All kinase in this family  FGFR3
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