Allelic Variants

There are no related allelic variants
Related diseases of KIF 1XBCA_STU (PDB code: 1XBC, chain A)
Number of involved diseases in the family 105
Number of FGR related diseases 1
All kinase in this family  FGR
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
n/aEpstein-Barr virus infectionFGR, JAK1, JAK3, LYN,
PRKACG, SYK, TYK2
16Link
Prostate cancerCHEK2, EGFR, EPHB2, FGFR1,
FGFR2, PDGFRA, PDGFRB
42Link
n/aMeaslesFYN, JAK1, JAK2, JAK3, TYK216Link
LeukemiaABL1, ABL2, JAK2, KIT,
PDGFRB
15Link
Lung cancerALK, EGFR, PTK2, ROS140Link
n/aEpithelial cell signaling in Helicobacter pylori infectionCSK, EGFR, LYN, SRC41Link
n/aTuberculosisJAK1, JAK2, SRC, SYK21Link
MelanomaEGFR, FGFR1, PDGFRA, PDGFRB41Link
n/aInfluenza AJAK1, JAK2, PRKCA, TYK259Link
n/aAmoebiasisPRKACG, PRKCA, PTK257Link
n/aHerpes simplex infectionJAK1, JAK2, TYK210Link
n/aImmunodeficienciesJAK3, LCK, ZAP7016Link
n/aGliomaEGFR, PDGFRA, PDGFRB41Link
n/aToxoplasmosisJAK1, JAK2, TYK210Link
n/aPathogenic Escherichia coli infectionABL1, FYN, PRKCA61Link
NeuroblastomaALK, NTRK2, NTRK310Link
n/aHepatitis CEGFR, JAK1, TYK240Link
n/aViral myocarditisABL1, ABL2, FYN13Link
Crouzon syndromeFGFR2, FGFR38Link
Gastrointestinal stromal tumorKIT, PDGFRA12Link
n/aMyeloproliferative disorderJAK2, PDGFRB12Link
n/aPrion diseasesFYN, PRKACG10Link
LADD syndromeFGFR2, FGFR38Link
n/aLeishmaniasisJAK1, JAK210Link
Jackson-Weiss syndromeFGFR1, FGFR29Link
Pfeiffer syndromeFGFR1, FGFR29Link
SCIDJAK3, LCK16Link
Gastric cancerEGFR, FGFR239Link
n/aVibrio cholerae infectionPRKACG, PRKCA55Link
n/aChoriocarcinomaCSF1R, EGFR43Link
n/aShigellosisABL1, SRC20Link
n/aCervical cancerEGFR, FGFR338Link
n/aBladder cancerEGFR, FGFR338Link
Bent bone dysplasia syndromeFGFR28Link
Beare-Stevenson cutis gyrata syndromeFGFR28Link
n/aAgammaglobulinemia and isolated hormone deficiencyBTK5Link
AgammaglobulinemiaBTK5Link
n/aPituitary DwarfismBTK5Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR28Link
Apert syndromeFGFR28Link
ScaphocephalyFGFR28Link
n/aSaethre-Chotzen syndromeFGFR28Link
n/aMaturity onset diabetes of the youngBLK8Link
n/aAgammaglobulinemiasBTK5Link
CraniosynostosisFGFR28Link
Li-Fraumeni syndromeCHEK25Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR28Link
Osteoglophonic dysplasiaFGFR19Link
Hypogonadotropic hypogonadismFGFR19Link
n/aEsophageal cancerEGFR38Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR28Link
Adenocarcinoma of lungEGFR38Link
TrigonocephalyFGFR19Link
n/aOral cancerEGFR38Link
n/aLaryngeal cancerEGFR38Link
Kallmann syndromeFGFR19Link
Breast cancerCHEK25Link
n/aLeukoencephalopathy, diffuse hereditary, with spheroidsCSF1R13Link
OsteosarcomaCHEK25Link
n/aNevusFGFR37Link
n/aMultiple myelomaFGFR37Link
n/aAfrican trypanosomiasisPRKCA55Link
n/aPituitary tumorPRKCA55Link
n/aThyroid cancerRET11Link
n/aCardiomyopathyPRKACG1Link
n/aCocaine addictionPRKACG1Link
n/aMyasthenic syndromeMUSK5Link
n/aAlcoholismNTRK29Link
n/aObesityNTRK29Link
n/aHypereosinophilic syndromePDGFRA10Link
n/aRenal agenesis and Renal adysplasiaRET11Link
Hirschsprung diseaseRET11Link
Colon cancerSRC19Link
n/aTransient erythroblastopenia of childhoodTEC2Link
n/aTyrosine kinase 2 deficiencyTYK28Link
Selective T-cell defectZAP7010Link
Renal agenesisRET11Link
PheochromocytomaRET11Link
n/aCongenital central hypoventilation syndromeRET11Link
Central hypoventilation syndromeRET11Link
n/aMedullary thyroid carcinomaRET11Link
Multiple endocrine neoplasiaRET11Link
n/aCongenital myasthenic syndromeMUSK5Link
Mastocytosis with associated hematologic disorderKIT12Link
n/aSpermatocytic seminomaFGFR37Link
n/aThanatophoric dysplasiaFGFR37Link
n/aCancer progression/metastasisFGFR43Link
n/aMuenke syndromeFGFR37Link
n/aHypochondroplasiaFGFR37Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR37Link
n/aCATSHL syndromeFGFR37Link
n/aAchondroplasiaFGFR37Link
Colorectal cancerFGFR37Link
n/aLeprechaunismINSR5Link
Rabson-Mendenhall syndromeINSR5Link
ThrombocythemiaJAK210Link
PiebaldismKIT12Link
n/aGerm cell tumorsKIT12Link
Mast cell leukemiaKIT12Link
MyelofibrosisJAK210Link
n/aBudd-Chiari syndromeJAK210Link
Diabetes mellitusINSR5Link
Hyperinsulinemic hypoglycemiaINSR5Link
Lymphoproliferative syndromeITK6Link
Polycythemia veraJAK210Link