Allelic Variants

There are no related allelic variants
Related diseases of KIF 2X9FA_X9F (PDB code: 2X9F, chain A)
Number of involved diseases in the family 86
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
n/aEpstein-Barr virus infectionFGR, IRAK1, LYN, RIPK1, SYK,
TYK2
4Link
LeukemiaABL1, ABL2, BRAF, JAK24Link
n/aMeaslesFYN, IRAK1, JAK2, TYK23Link
n/aTuberculosisIRAK1, JAK2, SRC, SYK4Link
Lung cancerALK, BRAF, ROS14Link
n/aHepatitis CBRAF, RIPK1, TYK23Link
Prostate cancerBRAF, FGFR1, FGFR24Link
n/aViral myocarditisABL1, ABL2, FYN4Link
n/aToxoplasmosisIRAK1, JAK2, TYK21Link
HemangiomaFLT4, KDR5Link
Colorectal cancerBRAF, FGFR34Link
n/aHerpes simplex infectionJAK2, TYK21Link
n/aInfluenza AJAK2, TYK21Link
n/aLeishmaniasisIRAK1, JAK21Link
MelanomaBRAF, FGFR13Link
n/aShigellosisABL1, SRC4Link
Crouzon syndromeFGFR2, FGFR34Link
LADD syndromeFGFR2, FGFR34Link
n/aThyroid cancerBRAF, RET4Link
n/aPathogenic Escherichia coli infectionABL1, FYN3Link
Pfeiffer syndromeFGFR1, FGFR24Link
n/aEpithelial cell signaling in Helicobacter pylori infectionLYN, SRC4Link
Jackson-Weiss syndromeFGFR1, FGFR24Link
Apert syndromeFGFR24Link
Kallmann syndromeFGFR13Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR24Link
CraniosynostosisFGFR24Link
Bent bone dysplasia syndromeFGFR24Link
Beare-Stevenson cutis gyrata syndromeFGFR24Link
Gastric cancerFGFR24Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR24Link
n/aSpondylometaepiphyseal dysplasiaDDR24Link
TrigonocephalyFGFR13Link
n/aAlcoholismBRAF3Link
Adenocarcinoma of lungBRAF3Link
n/aNoonan syndrome and related disordersBRAF3Link
n/aMalignant melanomaBRAF3Link
NeuroblastomaALK3Link
n/aMaturity onset diabetes of the youngBLK3Link
Cardiofaciocutaneous syndromeBRAF3Link
LEOPARD syndromeBRAF3Link
Hypogonadotropic hypogonadismFGFR13Link
Osteoglophonic dysplasiaFGFR13Link
n/aSaethre-Chotzen syndromeFGFR24Link
n/aLeukoencephalopathy, diffuse hereditary, with spheroidsCSF1R5Link
Noonan syndromeBRAF3Link
n/aChoriocarcinomaCSF1R5Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR34Link
ScaphocephalyFGFR24Link
n/aRenal agenesis and Renal adysplasiaRET4Link
Hirschsprung diseaseRET4Link
SCIDLCK4Link
n/aImmunodeficienciesLCK4Link
MyelofibrosisJAK21Link
n/aMyeloproliferative disorderJAK21Link
ThrombocythemiaJAK21Link
n/aCongenital central hypoventilation syndromeRET4Link
Central hypoventilation syndromeRET4Link
Venous malformationsTEK1Link
n/aRheumatoid arthritisTEK1Link
n/aTyrosine kinase 2 deficiencyTYK21Link
Colon cancerSRC4Link
Renal agenesisRET4Link
n/aMedullary thyroid carcinomaRET4Link
Multiple endocrine neoplasiaRET4Link
PheochromocytomaRET4Link
n/aBudd-Chiari syndromeJAK21Link
Polycythemia veraJAK21Link
n/aCervical cancerFGFR34Link
n/aHypochondroplasiaFGFR34Link
n/aMuenke syndromeFGFR34Link
n/aAchondroplasiaFGFR34Link
n/aCATSHL syndromeFGFR34Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR24Link
n/aMultiple myelomaFGFR34Link
n/aBladder cancerFGFR34Link
n/aNevusFGFR34Link
n/aSpermatocytic seminomaFGFR34Link
n/aPertussisIRAK11Link
n/aChagas diseaseIRAK11Link
n/aAsthma susceptibilityIRAK33Link
n/aPrion diseasesFYN3Link
n/aLymphedemaFLT44Link
n/aThanatophoric dysplasiaFGFR34Link
n/aCancer progression/metastasisFGFR43Link
n/aLymphedemasFLT44Link