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 MAPK14 related diseases 12
All kinase in this family  MAPK14
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