Allelic Variants

There are no related allelic variants
Related diseases of KIF 3FQSA_585 (PDB code: 3FQS, chain A)
Number of involved diseases in the family 102
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 cancerBRAF, EGFR, EPHB2, FGFR1,
FGFR2, PDGFRA, PDGFRB
2Link
n/aEpstein-Barr virus infectionFGR, JAK1, JAK3, LYN, SYK,
TYK2
3Link
LeukemiaABL1, ABL2, BRAF, JAK2, KIT,
PDGFRB
1Link
Lung cancerALK, BRAF, EGFR, PTK2, ROS120Link
MelanomaBRAF, EGFR, FGFR1, PDGFRA,
PDGFRB
2Link
n/aMeaslesFYN, JAK1, JAK2, JAK3, TYK21Link
n/aTuberculosisJAK1, JAK2, SRC, SYK3Link
n/aHepatitis CBRAF, EGFR, JAK1, TYK22Link
n/aEpithelial cell signaling in Helicobacter pylori infectionCSK, EGFR, LYN, SRC2Link
n/aGliomaEGFR, PDGFRA, PDGFRB2Link
n/aViral myocarditisABL1, ABL2, FYN1Link
n/aToxoplasmosisJAK1, JAK2, TYK21Link
NeuroblastomaALK, NTRK2, NTRK33Link
n/aInfluenza AJAK1, JAK2, TYK21Link
n/aImmunodeficienciesJAK3, LCK, ZAP701Link
n/aHerpes simplex infectionJAK1, JAK2, TYK21Link
Crouzon syndromeFGFR2, FGFR31Link
Gastric cancerEGFR, FGFR22Link
n/aBladder cancerEGFR, FGFR32Link
n/aChoriocarcinomaCSF1R, EGFR2Link
n/aPathogenic Escherichia coli infectionABL1, FYN1Link
LADD syndromeFGFR2, FGFR31Link
Pfeiffer syndromeFGFR1, FGFR21Link
Jackson-Weiss syndromeFGFR1, FGFR21Link
n/aCervical cancerEGFR, FGFR32Link
n/aShigellosisABL1, SRC1Link
n/aLeishmaniasisJAK1, JAK21Link
Adenocarcinoma of lungBRAF, EGFR2Link
n/aThyroid cancerBRAF, RET1Link
Colorectal cancerBRAF, FGFR31Link
Gastrointestinal stromal tumorKIT, PDGFRA1Link
SCIDJAK3, LCK1Link
n/aAlcoholismBRAF, NTRK21Link
n/aMyeloproliferative disorderJAK2, PDGFRB1Link
Kallmann syndromeFGFR11Link
TrigonocephalyFGFR11Link
n/aMaturity onset diabetes of the youngBLK1Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR21Link
Osteoglophonic dysplasiaFGFR11Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR21Link
Bent bone dysplasia syndromeFGFR21Link
Beare-Stevenson cutis gyrata syndromeFGFR21Link
Apert syndromeFGFR21Link
n/aMalignant melanomaBRAF1Link
n/aLaryngeal cancerEGFR2Link
Hypogonadotropic hypogonadismFGFR11Link
n/aPituitary DwarfismBTK2Link
AgammaglobulinemiaBTK2Link
n/aAgammaglobulinemia and isolated hormone deficiencyBTK2Link
n/aLeukoencephalopathy, diffuse hereditary, with spheroidsCSF1R1Link
n/aNoonan syndrome and related disordersBRAF1Link
n/aOral cancerEGFR2Link
Cardiofaciocutaneous syndromeBRAF1Link
LEOPARD syndromeBRAF1Link
Noonan syndromeBRAF1Link
n/aEsophageal cancerEGFR2Link
n/aAgammaglobulinemiasBTK2Link
n/aMultiple myelomaFGFR31Link
CraniosynostosisFGFR21Link
n/aHypereosinophilic syndromePDGFRA1Link
n/aAmoebiasisPTK217Link
n/aRenal agenesis and Renal adysplasiaRET1Link
n/aObesityNTRK21Link
n/aMyasthenic syndromeMUSK1Link
n/aGerm cell tumorsKIT1Link
Mast cell leukemiaKIT1Link
Mastocytosis with associated hematologic disorderKIT1Link
n/aCongenital myasthenic syndromeMUSK1Link
Hirschsprung diseaseRET1Link
n/aCongenital central hypoventilation syndromeRET1Link
n/aTransient erythroblastopenia of childhoodTEC1Link
n/aTyrosine kinase 2 deficiencyTYK21Link
Selective T-cell defectZAP701Link
Colon cancerSRC1Link
Renal agenesisRET1Link
Central hypoventilation syndromeRET1Link
n/aMedullary thyroid carcinomaRET1Link
Multiple endocrine neoplasiaRET1Link
PheochromocytomaRET1Link
PiebaldismKIT1Link
ThrombocythemiaJAK21Link
n/aHypochondroplasiaFGFR31Link
n/aMuenke syndromeFGFR31Link
n/aNevusFGFR31Link
n/aAchondroplasiaFGFR31Link
n/aCATSHL syndromeFGFR31Link
n/aSaethre-Chotzen syndromeFGFR21Link
ScaphocephalyFGFR21Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR21Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR31Link
n/aSpermatocytic seminomaFGFR31Link
n/aThanatophoric dysplasiaFGFR31Link
Lymphoproliferative syndromeITK1Link
Polycythemia veraJAK21Link
n/aBudd-Chiari syndromeJAK21Link
MyelofibrosisJAK21Link
Hyperinsulinemic hypoglycemiaINSR8Link
Diabetes mellitusINSR8Link
n/aCancer progression/metastasisFGFR41Link
n/aPrion diseasesFYN1Link
n/aLeprechaunismINSR8Link
Rabson-Mendenhall syndromeINSR8Link