Allelic Variants

There are no related allelic variants
Related diseases of KIF 2JEDA_LG8 (PDB code: 2JED, chain A)
Number of involved diseases in the family 87
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, CSNK2A2, FGR,
GSK3B, JAK3, MAPK10, MAPK8
12Link
n/aMeaslesCDK2, CSNK2A2, FYN, GSK3B,
JAK2, JAK3, PRKCQ
6Link
n/aHerpes simplex infectionCDC2, CDK2, CSNK2A2, JAK2,
MAPK10, MAPK8
10Link
n/aTuberculosisCAMK2A, JAK2, MAPK10, MAPK8,
SRC
3Link
n/aInfluenza AGSK3B, JAK2, MAPK10, MAPK8,
PRKCB
4Link
Prostate cancerCDK2, FGFR2, GSK3B, PDPK14Link
n/aSalmonella infectionMAPK10, MAPK8, PKN1, PKN21Link
Diabetes mellitusMAPK10, MAPK8, PRKCD, PRKCE2Link
n/aShigellosisABL1, MAPK10, MAPK8, SRC3Link
NeuroblastomaNTRK1, NTRK2, NTRK32Link
n/aHepatitis CGSK3B, MAPK10, MAPK83Link
LeukemiaABL1, ABL2, JAK21Link
n/aToxoplasmosisJAK2, MAPK10, MAPK81Link
n/aEpithelial cell signaling in Helicobacter pylori infectionMAPK10, MAPK8, SRC3Link
n/aViral myocarditisABL1, ABL2, FYN1Link
n/aAlcoholismCAMKK1, CAMKK2, NTRK21Link
n/aLeishmaniasisJAK2, PRKCB2Link
n/aThyroid cancerNTRK1, RET3Link
n/aPertussisMAPK10, MAPK81Link
LADD syndromeFGFR2, FGFR31Link
n/aImmunodeficienciesJAK3, ZAP701Link
Crouzon syndromeFGFR2, FGFR31Link
n/aChagas diseaseMAPK10, MAPK81Link
n/aPathogenic Escherichia coli infectionABL1, FYN1Link
n/aMedullary thyroid carcinomaNTRK1, RET3Link
n/aAchondroplasiaFGFR31Link
ScaphocephalyFGFR21Link
n/aCervical cancerFGFR31Link
Colorectal cancerFGFR31Link
n/aHypochondroplasiaFGFR31Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR21Link
n/aMultiple myelomaFGFR31Link
n/aBladder cancerFGFR31Link
n/aMaturity onset diabetes of the youngBLK1Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR31Link
n/aCATSHL syndromeFGFR31Link
Jackson-Weiss syndromeFGFR21Link
n/aSaethre-Chotzen syndromeFGFR21Link
Apert syndromeFGFR21Link
Beare-Stevenson cutis gyrata syndromeFGFR21Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR21Link
Gastric cancerFGFR21Link
Venous malformationsTEK1Link
Lung cancerCDK22Link
Bent bone dysplasia syndromeFGFR21Link
n/aRheumatoid arthritisTEK1Link
Colon cancerSRC3Link
Pfeiffer syndromeFGFR21Link
CraniosynostosisFGFR21Link
Selective T-cell defectZAP701Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR21Link
n/aMuenke syndromeFGFR31Link
n/aCongenital stationary night blindnessGRK11Link
n/aNevusFGFR31Link
n/aVibrio cholerae infectionPRKCB1Link
n/aAfrican trypanosomiasisPRKCB1Link
Glycogen storage diseasePHKG21Link
n/aCirrhosis due to liver phosphorylase kinase deficiencyPHKG21Link
n/aObesityNTRK21Link
n/aGlycogen storage diseasesPHKG21Link
n/aAmoebiasisPRKCB1Link
n/aCerebral infarctionPRKCH1Link
Multiple endocrine neoplasiaRET3Link
PheochromocytomaRET3Link
Central hypoventilation syndromeRET3Link
n/aCongenital central hypoventilation syndromeRET3Link
n/aType I diabetes mellitusPRKCQ3Link
n/aRenal agenesis and Renal adysplasiaRET3Link
Hirschsprung diseaseRET3Link
n/aInsensitivity to painNTRK11Link
n/aEpileptic encephalopathyMAPK101Link
n/aOguchi diseaseGRK11Link
n/aBasal cell carcinomaGSK3B3Link
Renal agenesisRET3Link
n/aPrion diseasesFYN1Link
n/aSpermatocytic seminomaFGFR31Link
n/aThanatophoric dysplasiaFGFR31Link
n/aCancer progression/metastasisFGFR41Link
n/aEndocrine-cerebroosteodysplasiaICK1Link
Lymphoproliferative syndromeITK1Link
SCIDJAK31Link
n/aEarly infantile epileptic encephalopathyMAPK101Link
ThrombocythemiaJAK21Link
n/aMyeloproliferative disorderJAK21Link
Polycythemia veraJAK21Link
n/aBudd-Chiari syndromeJAK21Link
MyelofibrosisJAK21Link