Allelic Variants

There are no related allelic variants
Related diseases of KIF 2X9FA_X9F (PDB code: 2X9F, chain A)
Number of involved diseases in the family 86
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, IRAK1, LYN, RIPK1, SYK,
TYK2
4Link
LeukemiaABL1, ABL2, BRAF, JAK24Link
n/aMeaslesFYN, IRAK1, JAK2, TYK23Link
n/aTuberculosisIRAK1, JAK2, SRC, SYK4Link
Lung cancerALK, BRAF, ROS14Link
n/aHepatitis CBRAF, RIPK1, TYK23Link
Prostate cancerBRAF, FGFR1, FGFR24Link
n/aViral myocarditisABL1, ABL2, FYN4Link
n/aToxoplasmosisIRAK1, JAK2, TYK21Link
HemangiomaFLT4, KDR5Link
Colorectal cancerBRAF, FGFR34Link
n/aHerpes simplex infectionJAK2, TYK21Link
n/aInfluenza AJAK2, TYK21Link
n/aLeishmaniasisIRAK1, JAK21Link
MelanomaBRAF, FGFR13Link
n/aShigellosisABL1, SRC4Link
Crouzon syndromeFGFR2, FGFR34Link
LADD syndromeFGFR2, FGFR34Link
n/aThyroid cancerBRAF, RET4Link
n/aPathogenic Escherichia coli infectionABL1, FYN3Link
Pfeiffer syndromeFGFR1, FGFR24Link
n/aEpithelial cell signaling in Helicobacter pylori infectionLYN, SRC4Link
Jackson-Weiss syndromeFGFR1, FGFR24Link
Apert syndromeFGFR24Link
Kallmann syndromeFGFR13Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR24Link
CraniosynostosisFGFR24Link
Bent bone dysplasia syndromeFGFR24Link
Beare-Stevenson cutis gyrata syndromeFGFR24Link
Gastric cancerFGFR24Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR24Link
n/aSpondylometaepiphyseal dysplasiaDDR24Link
TrigonocephalyFGFR13Link
n/aAlcoholismBRAF3Link
Adenocarcinoma of lungBRAF3Link
n/aNoonan syndrome and related disordersBRAF3Link
n/aMalignant melanomaBRAF3Link
NeuroblastomaALK3Link
n/aMaturity onset diabetes of the youngBLK3Link
Cardiofaciocutaneous syndromeBRAF3Link
LEOPARD syndromeBRAF3Link
Hypogonadotropic hypogonadismFGFR13Link
Osteoglophonic dysplasiaFGFR13Link
n/aSaethre-Chotzen syndromeFGFR24Link
n/aLeukoencephalopathy, diffuse hereditary, with spheroidsCSF1R5Link
Noonan syndromeBRAF3Link
n/aChoriocarcinomaCSF1R5Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR34Link
ScaphocephalyFGFR24Link
n/aRenal agenesis and Renal adysplasiaRET4Link
Hirschsprung diseaseRET4Link
SCIDLCK4Link
n/aImmunodeficienciesLCK4Link
MyelofibrosisJAK21Link
n/aMyeloproliferative disorderJAK21Link
ThrombocythemiaJAK21Link
n/aCongenital central hypoventilation syndromeRET4Link
Central hypoventilation syndromeRET4Link
Venous malformationsTEK1Link
n/aRheumatoid arthritisTEK1Link
n/aTyrosine kinase 2 deficiencyTYK21Link
Colon cancerSRC4Link
Renal agenesisRET4Link
n/aMedullary thyroid carcinomaRET4Link
Multiple endocrine neoplasiaRET4Link
PheochromocytomaRET4Link
n/aBudd-Chiari syndromeJAK21Link
Polycythemia veraJAK21Link
n/aCervical cancerFGFR34Link
n/aHypochondroplasiaFGFR34Link
n/aMuenke syndromeFGFR34Link
n/aAchondroplasiaFGFR34Link
n/aCATSHL syndromeFGFR34Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR24Link
n/aMultiple myelomaFGFR34Link
n/aBladder cancerFGFR34Link
n/aNevusFGFR34Link
n/aSpermatocytic seminomaFGFR34Link
n/aPertussisIRAK11Link
n/aChagas diseaseIRAK11Link
n/aAsthma susceptibilityIRAK33Link
n/aPrion diseasesFYN3Link
n/aLymphedemaFLT44Link
n/aThanatophoric dysplasiaFGFR34Link
n/aCancer progression/metastasisFGFR43Link
n/aLymphedemasFLT44Link