Allelic Variants

There are no related allelic variants
Related diseases of KIF 3E92A_G6A (PDB code: 3E92, chain A)
Number of involved diseases in the family 55
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, CSNK2A2, FGR,
GSK3B, LYN, MAPK10, MAPK14,
MAPK8, MAPK9
54Link
Prostate cancerCDK2, EPHB2, FGFR1, FGFR2,
GSK3B, PDPK1
7Link
n/aHerpes simplex infectionCDC2, CDK2, CSNK2A2, MAPK10,
MAPK8, MAPK9
6Link
n/aEpithelial cell signaling in Helicobacter pylori infectionLYN, MAPK10, MAPK14, MAPK8,
MAPK9, SRC
50Link
n/aShigellosisABL1, MAPK10, MAPK14, MAPK8,
MAPK9, SRC
50Link
n/aInfluenza AGSK3B, MAPK10, MAPK14,
MAPK8, MAPK9
51Link
n/aTuberculosisMAPK10, MAPK14, MAPK8,
MAPK9, SRC
50Link
n/aHepatitis CGSK3B, MAPK10, MAPK14,
MAPK8, MAPK9
51Link
n/aPertussisMAPK10, MAPK14, MAPK8, MAPK948Link
n/aChagas diseaseMAPK10, MAPK14, MAPK8, MAPK948Link
n/aSalmonella infectionMAPK10, MAPK14, MAPK8, MAPK948Link
n/aToxoplasmosisMAPK10, MAPK14, MAPK8, MAPK948Link
n/aMeaslesCDK2, CSNK2A2, FYN, GSK3B7Link
Diabetes mellitusMAPK10, MAPK8, MAPK93Link
n/aViral myocarditisABL1, ABL2, FYN1Link
Pfeiffer syndromeFGFR1, FGFR21Link
Jackson-Weiss syndromeFGFR1, FGFR21Link
LeukemiaABL1, ABL21Link
n/aPathogenic Escherichia coli infectionABL1, FYN1Link
Kallmann syndromeFGFR11Link
Apert syndromeFGFR21Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR21Link
Gastric cancerFGFR21Link
n/aBladder cancerDAPK11Link
MelanomaFGFR11Link
Lung cancerCDK23Link
n/aMaturity onset diabetes of the youngBLK1Link
n/aCocaine addictionCDK51Link
Beare-Stevenson cutis gyrata syndromeFGFR21Link
TrigonocephalyFGFR11Link
Osteoglophonic dysplasiaFGFR11Link
Hypogonadotropic hypogonadismFGFR11Link
LADD syndromeFGFR21Link
Bent bone dysplasia syndromeFGFR21Link
n/aGlycogen storage diseasesPHKG21Link
n/aLeishmaniasisMAPK1447Link
n/aAmyotrophic lateral sclerosisMAPK1447Link
n/aCirrhosis due to liver phosphorylase kinase deficiencyPHKG21Link
Glycogen storage diseasePHKG21Link
Colon cancerSRC3Link
Mental retardationRPS6KA31Link
n/aCoffin-Lowry syndromeRPS6KA31Link
n/aNon-syndromic X-linked mental retardationRPS6KA31Link
n/aEpileptic encephalopathyMAPK102Link
n/aEarly infantile epileptic encephalopathyMAPK102Link
n/aSaethre-Chotzen syndromeFGFR21Link
Crouzon syndromeFGFR21Link
CraniosynostosisFGFR21Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR21Link
ScaphocephalyFGFR21Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR21Link
SCIDLCK6Link
n/aImmunodeficienciesLCK6Link
n/aBasal cell carcinomaGSK3B4Link
n/aPrion diseasesFYN1Link