Allelic Variants

There are no related allelic variants
Related diseases of KIF 2XYNA_VX6 (PDB code: 2XYN, chain A)
Number of involved diseases in the family 105
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 infectionCDC2, CDK2, FGR, JAK3, LYN,
MAPK14, RIPK1, SYK
19Link
LeukemiaABL1, ABL2, JAK2, KIT,
PDGFRB, TGFBR1
17Link
n/aMeaslesCDK2, FYN, IRAK4, JAK2,
JAK3, PRKCQ
34Link
Prostate cancerCDK2, EPHB2, FGFR1, FGFR2,
PDGFRA, PDGFRB
13Link
n/aTuberculosisIRAK4, JAK2, MAPK14, SRC,
SYK
27Link
n/aEpithelial cell signaling in Helicobacter pylori infectionCSK, LYN, MAPK14, SRC15Link
n/aLeishmaniasisIRAK4, JAK2, MAPK1416Link
n/aToxoplasmosisIRAK4, JAK2, MAPK1416Link
n/aInfluenza AIRAK4, JAK2, MAPK1416Link
n/aChagas diseaseIRAK4, MAPK14, TGFBR13Link
MelanomaFGFR1, PDGFRA, PDGFRB2Link
n/aHerpes simplex infectionCDC2, CDK2, JAK225Link
n/aSalmonella infectionMAPK14, PKN1, PKN24Link
Lung cancerALK, CDK2, ROS114Link
n/aViral myocarditisABL1, ABL2, FYN5Link
n/aShigellosisABL1, MAPK14, SRC17Link
n/aMyeloproliferative disorderJAK2, PDGFRB14Link
LADD syndromeFGFR2, FGFR32Link
n/aImmunodeficienciesJAK3, LCK9Link
n/aType I diabetes mellitusERBB3, PRKCQ10Link
Gastrointestinal stromal tumorKIT, PDGFRA3Link
n/aPathogenic Escherichia coli infectionABL1, FYN5Link
Crouzon syndromeFGFR2, FGFR32Link
n/aPertussisIRAK4, MAPK143Link
SCIDJAK3, LCK9Link
Colon cancerAURKA, SRC71Link
Jackson-Weiss syndromeFGFR1, FGFR22Link
n/aGliomaPDGFRA, PDGFRB2Link
n/aCardiomyopathyPRKAA1, PRKAA22Link
n/aHepatitis CMAPK14, RIPK14Link
Pfeiffer syndromeFGFR1, FGFR22Link
Kallmann syndromeFGFR12Link
Beare-Stevenson cutis gyrata syndromeFGFR22Link
Apert syndromeFGFR22Link
Gastric cancerFGFR22Link
Bent bone dysplasia syndromeFGFR22Link
CraniosynostosisFGFR22Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR22Link
TrigonocephalyFGFR12Link
Osteoglophonic dysplasiaFGFR12Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR22Link
n/aEpileptic encephalopathyCDKL51Link
Hypogonadotropic hypogonadismFGFR12Link
n/aAgammaglobulinemiasBTK2Link
n/aPituitary DwarfismBTK2Link
n/aChrondrodysplasiaBMPR1B1Link
BrachydactylyBMPR1B1Link
Fibrodysplasia ossificans progressivaACVR12Link
NeuroblastomaALK2Link
n/aMaturity onset diabetes of the youngBLK2Link
AgammaglobulinemiaBTK2Link
n/aAgammaglobulinemia and isolated hormone deficiencyBTK2Link
n/aLeukoencephalopathy, diffuse hereditary, with spheroidsCSF1R2Link
n/aLethal congenital contractural syndromeERBB31Link
n/aChoriocarcinomaCSF1R2Link
n/aAngelman syndrome-likeCDKL51Link
n/aCocaine addictionCDK51Link
n/aPrader-Willi and Angelman syndromesCDKL51Link
n/aEarly infantile epileptic encephalopathyCDKL51Link
n/aAchondroplasiaFGFR32Link
n/aSaethre-Chotzen syndromeFGFR22Link
n/aThyroid cancerRET3Link
n/aRenal agenesis and Renal adysplasiaRET3Link
Hirschsprung diseaseRET3Link
Diabetes mellitusPRKCD9Link
n/aHypereosinophilic syndromePDGFRA2Link
n/aGerm cell tumorsKIT3Link
Mast cell leukemiaKIT3Link
Mastocytosis with associated hematologic disorderKIT3Link
n/aAmyotrophic lateral sclerosisMAPK142Link
n/aCongenital central hypoventilation syndromeRET3Link
Central hypoventilation syndromeRET3Link
n/aRheumatoid arthritisTEK3Link
Loeys-Dietz syndromeTGFBR11Link
n/aFamilial thoracic aortic aneurysm and dissectionTGFBR11Link
Multiple self-healing squamous epitheliomaTGFBR11Link
Venous malformationsTEK3Link
n/aTransient erythroblastopenia of childhoodTEC1Link
n/aMedullary thyroid carcinomaRET3Link
Multiple endocrine neoplasiaRET3Link
PheochromocytomaRET3Link
Renal agenesisRET3Link
PiebaldismKIT3Link
ThrombocythemiaJAK214Link
n/aCervical cancerFGFR32Link
Colorectal cancerFGFR32Link
n/aHypochondroplasiaFGFR32Link
n/aCATSHL syndromeFGFR32Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR32Link
ScaphocephalyFGFR22Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR22Link
n/aMultiple myelomaFGFR32Link
n/aBladder cancerFGFR32Link
n/aMuenke syndromeFGFR32Link
n/aNevusFGFR32Link
Lymphoproliferative syndromeITK2Link
Polycythemia veraJAK214Link
n/aBudd-Chiari syndromeJAK214Link
MyelofibrosisJAK214Link
IRAK4 deficiencyIRAK41Link
n/aInvasive pneumococcal diseaseIRAK41Link
n/aSpermatocytic seminomaFGFR32Link
n/aThanatophoric dysplasiaFGFR32Link
n/aCancer progression/metastasisFGFR42Link
n/aPrion diseasesFYN2Link