Allelic Variants

There are no related allelic variants
Related diseases of KIF 1OUKA_084 (PDB code: 1OUK, chain A)
Number of involved diseases in the family 46
Number of GSK3A related diseases 0
All kinase in this family  GSK3A
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
n/aEpstein-Barr virus infectionCDC2, CDK2, FGR, GSK3B,
MAPK10, MAPK11, MAPK14,
MAPK8, MAPK9
121Link
n/aShigellosisMAPK10, MAPK11, MAPK14,
MAPK8, MAPK9, SRC
100Link
n/aTuberculosisMAPK10, MAPK11, MAPK14,
MAPK8, MAPK9, SRC
100Link
n/aInfluenza AGSK3B, MAPK10, MAPK11,
MAPK14, MAPK8, MAPK9
103Link
n/aEpithelial cell signaling in Helicobacter pylori infectionMAPK10, MAPK11, MAPK14,
MAPK8, MAPK9, SRC
100Link
n/aHepatitis CGSK3B, MAPK10, MAPK11,
MAPK14, MAPK8, MAPK9
103Link
n/aSalmonella infectionMAPK10, MAPK11, MAPK14,
MAPK8, MAPK9
98Link
n/aChagas diseaseMAPK10, MAPK11, MAPK14,
MAPK8, MAPK9
98Link
n/aPertussisMAPK10, MAPK11, MAPK14,
MAPK8, MAPK9
98Link
n/aHerpes simplex infectionCDC2, CDK2, MAPK10, MAPK8,
MAPK9
40Link
n/aToxoplasmosisMAPK10, MAPK11, MAPK14,
MAPK8, MAPK9
98Link
Prostate cancerCDK2, FGFR1, FGFR2, GSK3B13Link
Diabetes mellitusMAPK10, MAPK8, MAPK922Link
n/aMeaslesCDK2, FYN, GSK3B7Link
Jackson-Weiss syndromeFGFR1, FGFR26Link
Pfeiffer syndromeFGFR1, FGFR26Link
n/aLeishmaniasisMAPK11, MAPK1487Link
n/aAmyotrophic lateral sclerosisMAPK11, MAPK1487Link
Gastric cancerFGFR24Link
Kallmann syndromeFGFR12Link
Apert syndromeFGFR24Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR24Link
n/aCocaine addictionCDK51Link
MelanomaFGFR12Link
Lung cancerCDK22Link
Beare-Stevenson cutis gyrata syndromeFGFR24Link
Hypogonadotropic hypogonadismFGFR12Link
TrigonocephalyFGFR12Link
Osteoglophonic dysplasiaFGFR12Link
n/aSaethre-Chotzen syndromeFGFR24Link
Bent bone dysplasia syndromeFGFR24Link
n/aImmunodeficienciesLCK11Link
n/aBasal cell carcinomaGSK3B5Link
SCIDLCK11Link
n/aEarly infantile epileptic encephalopathyMAPK1011Link
Colon cancerSRC2Link
n/aEpileptic encephalopathyMAPK1011Link
n/aViral myocarditisFYN1Link
n/aPathogenic Escherichia coli infectionFYN1Link
CraniosynostosisFGFR24Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR24Link
Crouzon syndromeFGFR24Link
LADD syndromeFGFR24Link
n/aPrion diseasesFYN1Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR24Link
ScaphocephalyFGFR24Link