Allelic Variants

There are no related allelic variants
Related diseases of KIF 2BMCA_MPY (PDB code: 2BMC, 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/aEpstein-Barr virus infectionCDC2, CDK2, CSNK2A1,
CSNK2A2, GSK3B, JAK1, JAK3,
MAP2K4, MAPK10, MAPK8, RIPK1
21Link
n/aMeaslesCDK2, CDK4, CSNK2A1,
CSNK2A2, GSK3B, IRAK4, JAK1,
JAK2, JAK3, PRKCQ
37Link
n/aHerpes simplex infectionCDC2, CDK2, CSNK2A1,
CSNK2A2, JAK1, JAK2, MAPK10,
MAPK8
15Link
n/aInfluenza AGSK3B, IRAK4, JAK1, JAK2,
MAP2K4, MAPK10, MAPK8, RAF1
9Link
n/aHepatitis CEGFR, GSK3B, JAK1, MAPK10,
MAPK8, RAF1, RIPK1
10Link
n/aTuberculosisCAMK2A, IRAK4, JAK1, JAK2,
MAPK10, MAPK8, RAF1
3Link
Prostate cancerCDK2, EGFR, FGFR1, FGFR2,
GSK3B, PDPK1, RAF1
36Link
LeukemiaABL1, ABL2, CDK4, JAK2,
RAF1, RPS6KB1
26Link
Lung cancerALK, CDK2, CDK4, EGFR, PTK232Link
n/aToxoplasmosisIRAK4, JAK1, JAK2, MAPK10,
MAPK8
2Link
MelanomaCDK4, EGFR, FGFR1, RAF129Link
n/aAlcoholismCAMKK1, CAMKK2, NTRK2, RAF12Link
Diabetes mellitusMAPK10, MAPK8, PRKCD, PRKCZ6Link
n/aChagas diseaseIRAK4, MAP2K4, MAPK10, MAPK81Link
NeuroblastomaALK, NTRK1, NTRK2, NTRK33Link
n/aEpithelial cell signaling in Helicobacter pylori infectionEGFR, MAP2K4, MAPK10, MAPK83Link
n/aPertussisIRAK4, MAPK10, MAPK81Link
n/aSalmonella infectionMAPK10, MAPK8, PKN21Link
n/aCardiomyopathyMYLK2, PRKAA1, PRKAA21Link
n/aLeishmaniasisIRAK4, JAK1, JAK22Link
n/aImmunodeficienciesJAK3, LCK, ZAP7011Link
n/aCervical cancerCDK4, EGFR, FGFR323Link
n/aShigellosisABL1, MAPK10, MAPK84Link
Gastric cancerEGFR, FGFR23Link
Pfeiffer syndromeFGFR1, FGFR26Link
Jackson-Weiss syndromeFGFR1, FGFR26Link
n/aViral myocarditisABL1, ABL24Link
n/aThyroid cancerNTRK1, RET3Link
n/aBladder cancerEGFR, FGFR33Link
SCIDJAK3, LCK11Link
n/aMedullary thyroid carcinomaNTRK1, RET3Link
n/aGliomaCDK4, EGFR23Link
LADD syndromeFGFR2, FGFR32Link
Crouzon syndromeFGFR2, FGFR32Link
Beare-Stevenson cutis gyrata syndromeFGFR21Link
TrigonocephalyFGFR16Link
Bent bone dysplasia syndromeFGFR21Link
n/aPathogenic Escherichia coli infectionABL14Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR21Link
Kallmann syndromeFGFR16Link
Apert syndromeFGFR21Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR21Link
CraniosynostosisFGFR21Link
Colon cancerAURKA37Link
Osteoglophonic dysplasiaFGFR16Link
n/aSaethre-Chotzen syndromeFGFR21Link
n/aEsophageal cancerEGFR2Link
n/aOral cancerEGFR2Link
n/aAgammaglobulinemia and isolated hormone deficiencyBTK1Link
n/aMalignant melanomaCDK421Link
n/aCocaine addictionCDK52Link
n/aChoriocarcinomaEGFR2Link
n/aLaryngeal cancerEGFR2Link
n/aMaturity onset diabetes of the youngBLK1Link
Hypogonadotropic hypogonadismFGFR16Link
n/aAgammaglobulinemiasBTK1Link
Adenocarcinoma of lungEGFR2Link
AgammaglobulinemiaBTK1Link
n/aPituitary DwarfismBTK1Link
Colorectal cancerFGFR32Link
ScaphocephalyFGFR21Link
n/aCirrhosis due to liver phosphorylase kinase deficiencyPHKG21Link
Glycogen storage diseasePHKG21Link
n/aType I diabetes mellitusPRKCQ2Link
n/aAmoebiasisPTK21Link
n/aGlycogen storage diseasesPHKG21Link
n/aObesityNTRK21Link
n/aEpileptic encephalopathyMAPK101Link
n/aFamilial thoracic aortic aneurysm and dissectionMYLK1Link
n/aAortic aneurysmMYLK1Link
n/aInsensitivity to painNTRK12Link
LEOPARD syndromeRAF11Link
Noonan syndromeRAF11Link
Renal agenesisRET2Link
Venous malformationsTEK2Link
n/aRheumatoid arthritisTEK2Link
Selective T-cell defectZAP701Link
PheochromocytomaRET2Link
Multiple endocrine neoplasiaRET2Link
n/aRenal agenesis and Renal adysplasiaRET2Link
Hirschsprung diseaseRET2Link
n/aCongenital central hypoventilation syndromeRET2Link
Central hypoventilation syndromeRET2Link
n/aEarly infantile epileptic encephalopathyMAPK101Link
ThrombocythemiaJAK22Link
n/aMuenke syndromeFGFR32Link
n/aNevusFGFR32Link
n/aSpermatocytic seminomaFGFR32Link
n/aThanatophoric dysplasiaFGFR32Link
n/aHypochondroplasiaFGFR32Link
n/aAchondroplasiaFGFR32Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR21Link
n/aMultiple myelomaFGFR32Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR32Link
n/aCATSHL syndromeFGFR32Link
n/aCancer progression/metastasisFGFR41Link
n/aCongenital stationary night blindnessGRK11Link
Polycythemia veraJAK22Link
n/aBudd-Chiari syndromeJAK22Link
MyelofibrosisJAK22Link
n/aMyeloproliferative disorderJAK22Link
Lymphoproliferative syndromeITK5Link
IRAK4 deficiencyIRAK41Link
n/aOguchi diseaseGRK11Link
n/aBasal cell carcinomaGSK3B7Link
n/aEndocrine-cerebroosteodysplasiaICK1Link
n/aInvasive pneumococcal diseaseIRAK41Link