Allelic Variants

There are no related allelic variants
Related diseases of KIF 2XB7A_GUI (PDB code: 2XB7, chain A)
Number of involved diseases in the family 107
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/aMeaslesFYN, JAK1, JAK2, JAK3,
MAP3K7, TYK2
2Link
Prostate cancerEGFR, EPHB2, FGFR1, FGFR2,
IGF1R, INSRR
38Link
n/aEpstein-Barr virus infectionFGR, JAK1, JAK3, MAP3K7,
SYK, TYK2
2Link
n/aTuberculosisJAK1, JAK2, SRC, SYK2Link
MelanomaEGFR, FGFR1, IGF1R, MET39Link
n/aHerpes simplex infectionJAK1, JAK2, MAP3K7, TYK22Link
n/aToxoplasmosisJAK1, JAK2, MAP3K7, TYK22Link
Lung cancerALK, EGFR, PTK2, ROS110Link
n/aEpithelial cell signaling in Helicobacter pylori infectionCSK, EGFR, MET, SRC3Link
n/aHepatitis CEGFR, JAK1, TYK22Link
LeukemiaABL1, ABL2, JAK22Link
n/aViral myocarditisABL1, ABL2, FYN2Link
Gastric cancerEGFR, FGFR2, MET3Link
n/aLeishmaniasisJAK1, JAK2, MAP3K72Link
NeuroblastomaALK, NTRK1, NTRK210Link
n/aInfluenza AJAK1, JAK2, TYK22Link
n/aCervical cancerEGFR, FGFR31Link
Jackson-Weiss syndromeFGFR1, FGFR22Link
HemangiomaFLT4, KDR2Link
n/aImmunodeficienciesJAK3, ZAP7020Link
n/aBladder cancerEGFR, FGFR31Link
n/aPathogenic Escherichia coli infectionABL1, FYN2Link
n/aShigellosisABL1, SRC2Link
Colon cancerAURKA, SRC2Link
Pfeiffer syndromeFGFR1, FGFR22Link
n/aChoriocarcinomaCSF1R, EGFR1Link
n/aMedullary thyroid carcinomaNTRK1, RET2Link
LADD syndromeFGFR2, FGFR31Link
Crouzon syndromeFGFR2, FGFR31Link
n/aThyroid cancerNTRK1, RET2Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR21Link
Apert syndromeFGFR21Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR31Link
Beare-Stevenson cutis gyrata syndromeFGFR21Link
n/aMultiple myelomaFGFR31Link
n/aSaethre-Chotzen syndromeFGFR21Link
CraniosynostosisFGFR21Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR21Link
ScaphocephalyFGFR21Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR21Link
Bent bone dysplasia syndromeFGFR21Link
CataractEPHA21Link
Kallmann syndromeFGFR12Link
n/aLeukoencephalopathy, diffuse hereditary, with spheroidsCSF1R1Link
n/aSpondylometaepiphyseal dysplasiaDDR21Link
n/aAgammaglobulinemia and isolated hormone deficiencyBTK1Link
AgammaglobulinemiaBTK1Link
n/aMaturity onset diabetes of the youngBLK1Link
n/aAgammaglobulinemiasBTK1Link
n/aPituitary DwarfismBTK1Link
n/aOral cancerEGFR1Link
n/aEsophageal cancerEGFR1Link
Osteoglophonic dysplasiaFGFR12Link
TrigonocephalyFGFR12Link
Hypogonadotropic hypogonadismFGFR12Link
n/aCATSHL syndromeFGFR31Link
n/aGliomaEGFR1Link
n/aLaryngeal cancerEGFR1Link
Adenocarcinoma of lungEGFR1Link
n/aSpermatocytic seminomaFGFR31Link
n/aAchondroplasiaFGFR31Link
n/aCongenital myasthenic syndromeMUSK1Link
n/aMyasthenic syndromeMUSK1Link
n/aInsensitivity to painNTRK11Link
n/aAlcoholismNTRK22Link
Hepatocellular carcinomaMET3Link
n/aAutism suseptibilityMET3Link
Retinitis pigmentosaMERTK1Link
Renal cell carcinomaMET3Link
n/aCholangiocarcinomaMET3Link
n/aMalariaMET3Link
n/aObesityNTRK22Link
n/aAmoebiasisPTK21Link
Renal agenesisRET2Link
n/aTransient erythroblastopenia of childhoodTEC1Link
n/aTyrosine kinase 2 deficiencyTYK22Link
Selective T-cell defectZAP7020Link
PheochromocytomaRET2Link
Multiple endocrine neoplasiaRET2Link
n/aRenal agenesis and Renal adysplasiaRET2Link
Hirschsprung diseaseRET2Link
n/aCongenital central hypoventilation syndromeRET2Link
Central hypoventilation syndromeRET2Link
n/a46XY sex reversal 6MAP3K11Link
SCIDJAK31Link
n/aLymphedemasFLT41Link
n/aLymphedemaFLT41Link
n/aPrion diseasesFYN1Link
n/aMalignant pleural mesotheliomaIGF1R37Link
n/aCancer progression/metastasisFGFR41Link
n/aThanatophoric dysplasiaFGFR31Link
Colorectal cancerFGFR31Link
n/aHypochondroplasiaFGFR31Link
n/aMuenke syndromeFGFR31Link
n/aNevusFGFR31Link
n/aSynovial sarcomaIGF1R37Link
Insulin-like growth factor IIGF1R37Link
n/aBudd-Chiari syndromeJAK22Link
MyelofibrosisJAK22Link
n/aMyeloproliferative disorderJAK22Link
ThrombocythemiaJAK22Link
Polycythemia veraJAK22Link
Lymphoproliferative syndromeITK1Link
n/aLeprechaunismINSR11Link
Rabson-Mendenhall syndromeINSR11Link
Diabetes mellitusINSR11Link
Hyperinsulinemic hypoglycemiaINSR11Link