Allelic Variants

There are no related allelic variants
Related diseases of KIF 1M17A_AQ4 (PDB code: 1M17, chain A)
Number of involved diseases in the family 82
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
Prostate cancerEGFR, ERBB2, FGFR1, FGFR2,
IGF1R, PDGFRA, PDGFRB, PDPK1
98Link
MelanomaEGFR, FGFR1, IGF1R, PDGFRA,
PDGFRB
87Link
LeukemiaABL1, ABL2, JAK2, KIT,
PDGFRB
13Link
n/aEpithelial cell signaling in Helicobacter pylori infectionCSK, EGFR, LYN, SRC127Link
n/aEpstein-Barr virus infectionFGR, JAK3, LYN, SYK6Link
n/aTuberculosisJAK2, SRC, SYK58Link
Gastric cancerEGFR, ERBB2, FGFR279Link
n/aGliomaEGFR, PDGFRA, PDGFRB74Link
n/aMyeloproliferative disorderJAK2, PDGFRB3Link
Jackson-Weiss syndromeFGFR1, FGFR213Link
n/aCervical cancerEGFR, ERBB279Link
n/aBladder cancerEGFR, ERBB279Link
n/aMeaslesJAK2, JAK34Link
Lung cancerALK, EGFR74Link
n/aShigellosisABL1, SRC59Link
Adenocarcinoma of lungEGFR, ERBB279Link
n/aViral myocarditisABL1, ABL211Link
n/aChoriocarcinomaEGFR, ERBB279Link
Pfeiffer syndromeFGFR1, FGFR213Link
Colon cancerAURKA, SRC57Link
Gastrointestinal stromal tumorKIT, PDGFRA3Link
SCIDJAK3, LCK13Link
n/aImmunodeficienciesJAK3, LCK13Link
n/aPathogenic Escherichia coli infectionABL110Link
TrigonocephalyFGFR111Link
Breast cancerERBB215Link
Osteoglophonic dysplasiaFGFR111Link
GlioblastomaERBB215Link
n/aCholangiocarcinomaERBB215Link
Ovarian cancerERBB215Link
n/aLethal congenital contractural syndromeERBB31Link
Hypogonadotropic hypogonadismFGFR111Link
n/aType I diabetes mellitusERBB31Link
n/aHepatitis CEGFR74Link
Endometrial CancerERBB215Link
n/aMaturity onset diabetes of the youngBLK2Link
n/aAgammaglobulinemia and isolated hormone deficiencyBTK1Link
AgammaglobulinemiaBTK1Link
n/aPituitary DwarfismBTK1Link
n/aOral cancerEGFR74Link
n/aEsophageal cancerEGFR74Link
n/aPancreatic cancerERBB215Link
n/aAgammaglobulinemiasBTK1Link
n/aLaryngeal cancerEGFR74Link
NeuroblastomaALK2Link
Apert syndromeFGFR22Link
Kallmann syndromeFGFR111Link
Mastocytosis with associated hematologic disorderKIT3Link
n/aHypereosinophilic syndromePDGFRA2Link
Mast cell leukemiaKIT3Link
n/aGerm cell tumorsKIT3Link
MyelofibrosisJAK22Link
ThrombocythemiaJAK22Link
PiebaldismKIT3Link
n/aThyroid cancerRET4Link
n/aRenal agenesis and Renal adysplasiaRET4Link
PheochromocytomaRET4Link
Renal agenesisRET4Link
Multiple endocrine neoplasiaRET4Link
n/aMedullary thyroid carcinomaRET4Link
Hirschsprung diseaseRET4Link
n/aCongenital central hypoventilation syndromeRET4Link
Central hypoventilation syndromeRET4Link
n/aBudd-Chiari syndromeJAK22Link
n/aHerpes simplex infectionJAK22Link
Crouzon syndromeFGFR22Link
LADD syndromeFGFR22Link
CraniosynostosisFGFR22Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR22Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR22Link
Beare-Stevenson cutis gyrata syndromeFGFR22Link
Bent bone dysplasia syndromeFGFR22Link
n/aSaethre-Chotzen syndromeFGFR22Link
ScaphocephalyFGFR22Link
n/aLeishmaniasisJAK22Link
n/aToxoplasmosisJAK22Link
n/aInfluenza AJAK22Link
Polycythemia veraJAK22Link
Insulin-like growth factor IIGF1R2Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR22Link
n/aMalignant pleural mesotheliomaIGF1R2Link
n/aSynovial sarcomaIGF1R2Link