Allelic Variants

There are no related allelic variants
Related diseases of KIF 2WKMA_PFY (PDB code: 2WKM, chain A)
Number of involved diseases in the family 98
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/aMeaslesIRAK1, IRAK4, JAK1, JAK2,
JAK3, MAP3K7
6Link
n/aToxoplasmosisIRAK1, IRAK4, JAK1, JAK2,
MAP3K7
6Link
n/aLeishmaniasisIRAK1, IRAK4, JAK1, JAK2,
MAP3K7
6Link
n/aEpstein-Barr virus infectionIRAK1, JAK1, JAK3, MAP3K76Link
Lung cancerALK, EGFR, PTK2, ROS117Link
n/aTuberculosisIRAK1, IRAK4, JAK1, JAK26Link
Prostate cancerEGFR, FGFR1, FGFR217Link
MelanomaEGFR, FGFR1, MET22Link
n/aInfluenza AIRAK4, JAK1, JAK26Link
Gastric cancerEGFR, FGFR2, MET20Link
n/aHerpes simplex infectionJAK1, JAK2, MAP3K76Link
NeuroblastomaALK, NTRK2, NTRK37Link
n/aHepatitis CEGFR, JAK114Link
n/aChagas diseaseIRAK1, IRAK45Link
LADD syndromeFGFR2, FGFR35Link
HemangiomaFLT4, KDR21Link
Jackson-Weiss syndromeFGFR1, FGFR29Link
n/aPertussisIRAK1, IRAK45Link
Pfeiffer syndromeFGFR1, FGFR29Link
Crouzon syndromeFGFR2, FGFR35Link
n/aChoriocarcinomaCSF1R, EGFR17Link
n/aCervical cancerEGFR, FGFR316Link
n/aBladder cancerEGFR, FGFR316Link
LeukemiaABL1, JAK27Link
n/aEpithelial cell signaling in Helicobacter pylori infectionEGFR, MET19Link
Beare-Stevenson cutis gyrata syndromeFGFR24Link
Apert syndromeFGFR24Link
n/aMultiple myelomaFGFR35Link
n/aPathogenic Escherichia coli infectionABL16Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR35Link
Bent bone dysplasia syndromeFGFR24Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR24Link
ScaphocephalyFGFR24Link
n/aSaethre-Chotzen syndromeFGFR24Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR24Link
CraniosynostosisFGFR24Link
n/aAgammaglobulinemiasBTK1Link
n/aShigellosisABL16Link
AgammaglobulinemiaBTK1Link
Adenocarcinoma of lungEGFR13Link
n/aAgammaglobulinemia and isolated hormone deficiencyBTK1Link
n/aLaryngeal cancerEGFR13Link
n/aOral cancerEGFR13Link
n/aEsophageal cancerEGFR13Link
n/aGliomaEGFR13Link
Hypogonadotropic hypogonadismFGFR18Link
Osteoglophonic dysplasiaFGFR18Link
n/aLeukoencephalopathy, diffuse hereditary, with spheroidsCSF1R6Link
n/aViral myocarditisABL16Link
n/aPituitary DwarfismBTK1Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR24Link
TrigonocephalyFGFR18Link
n/aCATSHL syndromeFGFR35Link
Kallmann syndromeFGFR18Link
n/aNevusFGFR35Link
n/aAchondroplasiaFGFR35Link
n/aMyasthenic syndromeMUSK2Link
n/aAlcoholismNTRK26Link
n/aObesityNTRK26Link
n/aCongenital myasthenic syndromeMUSK2Link
Hepatocellular carcinomaMET8Link
Renal cell carcinomaMET8Link
n/aCholangiocarcinomaMET8Link
n/aMalariaMET8Link
n/aAutism suseptibilityMET8Link
n/aAmoebiasisPTK25Link
n/aThyroid cancerRET7Link
PheochromocytomaRET7Link
Renal agenesisRET7Link
n/aPopliteal pterygium syndromeRIPK42Link
Multiple endocrine neoplasiaRET7Link
n/aMedullary thyroid carcinomaRET7Link
n/aRenal agenesis and Renal adysplasiaRET7Link
Hirschsprung diseaseRET7Link
n/aCongenital central hypoventilation syndromeRET7Link
Central hypoventilation syndromeRET7Link
SCIDJAK35Link
n/aImmunodeficienciesJAK35Link
n/aLymphedemasFLT45Link
n/aLymphedemaFLT45Link
n/aLeprechaunismINSR4Link
n/aCancer progression/metastasisFGFR41Link
n/aThanatophoric dysplasiaFGFR35Link
Colorectal cancerFGFR35Link
n/aHypochondroplasiaFGFR35Link
n/aMuenke syndromeFGFR35Link
n/aSpermatocytic seminomaFGFR35Link
Rabson-Mendenhall syndromeINSR4Link
Diabetes mellitusINSR4Link
MyelofibrosisJAK24Link
n/aMyeloproliferative disorderJAK24Link
ThrombocythemiaJAK24Link
n/aBudd-Chiari syndromeJAK24Link
Polycythemia veraJAK24Link
Hyperinsulinemic hypoglycemiaINSR4Link
n/aInvasive pneumococcal diseaseIRAK44Link
IRAK4 deficiencyIRAK44Link
Lymphoproliferative syndromeITK4Link