Allelic Variants

There are no related allelic variants
Related diseases of KIF 3HA8A_5JZ (PDB code: 3HA8, chain A)
Number of involved diseases in the family 62
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 infectionCDK2, CSNK2A1, FGR, GSK3B,
LYN, MAPK10, MAPK14, MAPK8,
PRKACA, PRKACB, PRKX
52Link
Prostate cancerCDK2, CHEK2, FGFR1, FGFR2,
GSK3B, PDPK1
10Link
n/aEpithelial cell signaling in Helicobacter pylori infectionLYN, MAPK10, MAPK14, MAPK8,
SRC
57Link
n/aTuberculosisCAMK2D, MAPK10, MAPK14,
MAPK8, SRC
57Link
n/aShigellosisABL1, MAPK10, MAPK14, MAPK8,
SRC
57Link
n/aHerpes simplex infectionCDK2, CSNK2A1, MAPK10, MAPK84Link
n/aMeaslesCDK2, CSNK2A1, FYN, GSK3B4Link
n/aPrion diseasesFYN, PRKACA, PRKACB, PRKX1Link
n/aHepatitis CGSK3B, MAPK10, MAPK14, MAPK848Link
n/aInfluenza AGSK3B, MAPK10, MAPK14, MAPK848Link
n/aChagas diseaseMAPK10, MAPK14, MAPK848Link
n/aToxoplasmosisMAPK10, MAPK14, MAPK848Link
n/aPertussisMAPK10, MAPK14, MAPK848Link
n/aSalmonella infectionMAPK10, MAPK14, MAPK848Link
n/aVibrio cholerae infectionPRKACA, PRKACB, PRKX1Link
n/aAmoebiasisPRKACA, PRKACB, PRKX1Link
n/aCardiomyopathyPRKACA, PRKACB, PRKX1Link
n/aCocaine addictionPRKACA, PRKACB, PRKX1Link
n/aPathogenic Escherichia coli infectionABL1, FYN3Link
Jackson-Weiss syndromeFGFR1, FGFR26Link
Pfeiffer syndromeFGFR1, FGFR26Link
Diabetes mellitusMAPK10, MAPK81Link
n/aViral myocarditisABL1, FYN3Link
TrigonocephalyFGFR16Link
Kallmann syndromeFGFR16Link
MelanomaFGFR16Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR21Link
Gastric cancerFGFR21Link
n/aMaturity onset diabetes of the youngBLK1Link
Osteoglophonic dysplasiaFGFR16Link
Apert syndromeFGFR21Link
Li-Fraumeni syndromeCHEK21Link
Breast cancerCHEK21Link
OsteosarcomaCHEK21Link
Lung cancerCDK23Link
Hypogonadotropic hypogonadismFGFR16Link
n/aBladder cancerDAPK11Link
LADD syndromeFGFR21Link
Beare-Stevenson cutis gyrata syndromeFGFR21Link
n/aCirrhosis due to liver phosphorylase kinase deficiencyPHKG21Link
n/aGlycogen storage diseasesPHKG21Link
n/aLeishmaniasisMAPK1447Link
n/aAmyotrophic lateral sclerosisMAPK1447Link
Glycogen storage diseasePHKG21Link
n/aAlcoholismPRKACA1Link
Colon cancerSRC10Link
Mental retardationRPS6KA31Link
n/aCoffin-Lowry syndromeRPS6KA31Link
n/aNon-syndromic X-linked mental retardationRPS6KA31Link
n/aEpileptic encephalopathyMAPK101Link
n/aEarly infantile epileptic encephalopathyMAPK101Link
Crouzon syndromeFGFR21Link
CraniosynostosisFGFR21Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR21Link
Bent bone dysplasia syndromeFGFR21Link
LeukemiaABL13Link
n/aSaethre-Chotzen syndromeFGFR21Link
SCIDLCK30Link
n/aImmunodeficienciesLCK30Link
n/aBasal cell carcinomaGSK3B1Link
ScaphocephalyFGFR21Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR21Link