Allelic Variants

There are no related allelic variants
Related diseases of KIF 3A4OX_STU (PDB code: 3A4O, chain X)
Number of involved diseases in the family 88
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 cancerCDK2, EGFR, EPHB2, FGFR1,
FGFR2, PDGFRA, PDGFRB, PDPK1
44Link
n/aEpstein-Barr virus infectionCDC2, CDK2, FGR, LYN,
MAPK14, SYK
15Link
n/aEpithelial cell signaling in Helicobacter pylori infectionCSK, EGFR, LYN, MAPK14, SRC41Link
LeukemiaABL1, ABL2, JAK2, KIT,
PDGFRB
15Link
MelanomaEGFR, FGFR1, PDGFRA, PDGFRB41Link
n/aTuberculosisJAK2, MAPK14, SRC, SYK21Link
n/aBladder cancerDAPK1, EGFR, FGFR339Link
n/aMeaslesCDK2, FYN, JAK214Link
n/aGliomaEGFR, PDGFRA, PDGFRB41Link
n/aHerpes simplex infectionCDC2, CDK2, JAK214Link
Lung cancerCDK2, EGFR, PTK242Link
n/aInfluenza AJAK2, MAPK14, PRKCA59Link
n/aPathogenic Escherichia coli infectionABL1, FYN, PRKCA61Link
n/aShigellosisABL1, MAPK14, SRC20Link
n/aViral myocarditisABL1, ABL2, FYN13Link
n/aCervical cancerEGFR, FGFR338Link
n/aSalmonella infectionMAPK14, PKN112Link
n/aLeishmaniasisJAK2, MAPK1411Link
n/aHepatitis CEGFR, MAPK1439Link
n/aToxoplasmosisJAK2, MAPK1411Link
Crouzon syndromeFGFR2, FGFR38Link
LADD syndromeFGFR2, FGFR38Link
Pfeiffer syndromeFGFR1, FGFR29Link
Jackson-Weiss syndromeFGFR1, FGFR29Link
Gastric cancerEGFR, FGFR239Link
Gastrointestinal stromal tumorKIT, PDGFRA12Link
n/aChoriocarcinomaCSF1R, EGFR43Link
n/aMyeloproliferative disorderJAK2, PDGFRB12Link
n/aImmunodeficienciesLCK, ZAP7011Link
n/aAmoebiasisPRKCA, PTK257Link
Kallmann syndromeFGFR19Link
n/aPituitary DwarfismBTK5Link
n/aAgammaglobulinemiasBTK5Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR28Link
TrigonocephalyFGFR19Link
Apert syndromeFGFR28Link
n/aAgammaglobulinemia and isolated hormone deficiencyBTK5Link
AgammaglobulinemiaBTK5Link
Hypogonadotropic hypogonadismFGFR19Link
Osteoglophonic dysplasiaFGFR19Link
n/aOral cancerEGFR38Link
n/aMaturity onset diabetes of the youngBLK8Link
Fibrodysplasia ossificans progressivaACVR13Link
n/aEsophageal cancerEGFR38Link
n/aLeukoencephalopathy, diffuse hereditary, with spheroidsCSF1R13Link
Beare-Stevenson cutis gyrata syndromeFGFR28Link
Adenocarcinoma of lungEGFR38Link
n/aCocaine addictionCDK55Link
n/aLaryngeal cancerEGFR38Link
n/aSaethre-Chotzen syndromeFGFR28Link
Bent bone dysplasia syndromeFGFR28Link
SCIDLCK11Link
REtinitis pigmentosaMAK1Link
Mastocytosis with associated hematologic disorderKIT12Link
Mast cell leukemiaKIT12Link
ThrombocythemiaJAK210Link
PiebaldismKIT12Link
n/aGerm cell tumorsKIT12Link
n/aAmyotrophic lateral sclerosisMAPK141Link
n/aPertussisMAPK141Link
Diabetes mellitusPRKCE11Link
Colon cancerSRC19Link
Selective T-cell defectZAP7010Link
n/aPituitary tumorPRKCA55Link
n/aAfrican trypanosomiasisPRKCA55Link
n/aChagas diseaseMAPK141Link
n/aHypereosinophilic syndromePDGFRA10Link
n/aVibrio cholerae infectionPRKCA55Link
MyelofibrosisJAK210Link
n/aBudd-Chiari syndromeJAK210Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR37Link
n/aCATSHL syndromeFGFR37Link
n/aAchondroplasiaFGFR37Link
n/aMultiple myelomaFGFR37Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR28Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR28Link
CraniosynostosisFGFR28Link
ScaphocephalyFGFR28Link
Colorectal cancerFGFR37Link
n/aHypochondroplasiaFGFR37Link
n/aPrion diseasesFYN10Link
n/aEndocrine-cerebroosteodysplasiaICK2Link
Polycythemia veraJAK210Link
n/aCancer progression/metastasisFGFR43Link
n/aThanatophoric dysplasiaFGFR37Link
n/aMuenke syndromeFGFR37Link
n/aNevusFGFR37Link
n/aSpermatocytic seminomaFGFR37Link