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 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, 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