Allelic Variants

There are no related allelic variants
Related diseases of KIF 2ITYA_IRE (PDB code: 2ITY, chain A)
Number of involved diseases in the family 99
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, EPHB2, FGFR1, FGFR2,
INSRR
171Link
n/aEpstein-Barr virus infectionFGR, JAK3, MAP3K7, SYK10Link
n/aEpithelial cell signaling in Helicobacter pylori infectionCSK, EGFR, MET, SRC285Link
NeuroblastomaALK, NTRK1, NTRK2, NTRK310Link
n/aMeaslesFYN, JAK2, JAK3, MAP3K79Link
LeukemiaABL1, ABL2, JAK222Link
MelanomaEGFR, FGFR1, MET171Link
n/aTuberculosisJAK2, SRC, SYK132Link
Gastric cancerEGFR, FGFR2, MET166Link
Lung cancerALK, EGFR, PTK2169Link
n/aViral myocarditisABL1, ABL2, FYN22Link
n/aPathogenic Escherichia coli infectionABL1, FYN22Link
Colon cancerAURKA, SRC138Link
SCIDJAK3, LCK23Link
Pfeiffer syndromeFGFR1, FGFR229Link
n/aHerpes simplex infectionJAK2, MAP3K73Link
n/aCervical cancerEGFR, FGFR3166Link
n/aShigellosisABL1, SRC133Link
Jackson-Weiss syndromeFGFR1, FGFR229Link
n/aLeishmaniasisJAK2, MAP3K73Link
n/aToxoplasmosisJAK2, MAP3K73Link
n/aImmunodeficienciesJAK3, LCK23Link
n/aThyroid cancerNTRK1, RET10Link
n/aBladder cancerEGFR, FGFR3166Link
LADD syndromeFGFR2, FGFR34Link
n/aChoriocarcinomaCSF1R, EGFR174Link
Crouzon syndromeFGFR2, FGFR34Link
n/aMedullary thyroid carcinomaNTRK1, RET10Link
Apert syndromeFGFR24Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR24Link
Osteoglophonic dysplasiaFGFR129Link
TrigonocephalyFGFR129Link
CraniosynostosisFGFR24Link
Bent bone dysplasia syndromeFGFR24Link
Beare-Stevenson cutis gyrata syndromeFGFR24Link
Kallmann syndromeFGFR129Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR24Link
n/aSaethre-Chotzen syndromeFGFR24Link
Hypogonadotropic hypogonadismFGFR129Link
n/aAgammaglobulinemia and isolated hormone deficiencyBTK7Link
n/aLeukoencephalopathy, diffuse hereditary, with spheroidsCSF1R13Link
AgammaglobulinemiaBTK7Link
n/aPituitary DwarfismBTK7Link
n/aMaturity onset diabetes of the youngBLK11Link
n/aAgammaglobulinemiasBTK7Link
n/aSpondylometaepiphyseal dysplasiaDDR24Link
n/aOral cancerEGFR166Link
n/aType I diabetes mellitusERBB35Link
n/aLethal congenital contractural syndromeERBB35Link
Adenocarcinoma of lungEGFR166Link
n/aHepatitis CEGFR166Link
n/aEsophageal cancerEGFR166Link
n/aGliomaEGFR166Link
n/aLaryngeal cancerEGFR166Link
n/aAchondroplasiaFGFR33Link
ScaphocephalyFGFR24Link
n/aAlcoholismNTRK22Link
n/aObesityNTRK22Link
n/aAmoebiasisPTK22Link
n/aInsensitivity to painNTRK12Link
Hepatocellular carcinomaMET8Link
Renal cell carcinomaMET8Link
n/aCholangiocarcinomaMET8Link
n/aMalariaMET8Link
n/aAutism suseptibilityMET8Link
n/aRenal agenesis and Renal adysplasiaRET9Link
Hirschsprung diseaseRET9Link
n/aTransient erythroblastopenia of childhoodTEC4Link
Venous malformationsTEK11Link
n/aRheumatoid arthritisTEK11Link
n/aPopliteal pterygium syndromeRIPK41Link
Renal agenesisRET9Link
n/aCongenital central hypoventilation syndromeRET9Link
Central hypoventilation syndromeRET9Link
Multiple endocrine neoplasiaRET9Link
PheochromocytomaRET9Link
ThrombocythemiaJAK21Link
n/aMyeloproliferative disorderJAK21Link
n/aMuenke syndromeFGFR33Link
n/aNevusFGFR33Link
n/aSpermatocytic seminomaFGFR33Link
n/aHypochondroplasiaFGFR33Link
Colorectal cancerFGFR33Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR24Link
n/aMultiple myelomaFGFR33Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR33Link
n/aCATSHL syndromeFGFR33Link
n/aThanatophoric dysplasiaFGFR33Link
n/aCancer progression/metastasisFGFR41Link
Polycythemia veraJAK21Link
n/aInfluenza AJAK21Link
n/aBudd-Chiari syndromeJAK21Link
MyelofibrosisJAK21Link
Lymphoproliferative syndromeITK3Link
Hyperinsulinemic hypoglycemiaINSR3Link
n/aPrion diseasesFYN8Link
n/aLeprechaunismINSR3Link
Rabson-Mendenhall syndromeINSR3Link
Diabetes mellitusINSR3Link