Allelic Variants

There are no related allelic variants
Related diseases of KIF 2ZB1A_GK4 (PDB code: 2ZB1, chain A)
Number of involved diseases in the family 54
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, CSNK2A2, FGR, GSK3B,
LYN, MAPK10, MAPK11, MAPK14,
MAPK8, MAPK9
52Link
n/aEpithelial cell signaling in Helicobacter pylori infectionLYN, MAPK10, MAPK11, MAPK14,
MAPK8, MAPK9, SRC
48Link
n/aShigellosisABL1, MAPK10, MAPK11,
MAPK14, MAPK8, MAPK9, SRC
48Link
Prostate cancerCDK2, EPHB2, FGFR1, FGFR2,
GSK3B, PDPK1
7Link
n/aTuberculosisMAPK10, MAPK11, MAPK14,
MAPK8, MAPK9, SRC
48Link
n/aHepatitis CGSK3B, MAPK10, MAPK11,
MAPK14, MAPK8, MAPK9
49Link
n/aInfluenza AGSK3B, MAPK10, MAPK11,
MAPK14, MAPK8, MAPK9
49Link
n/aPertussisMAPK10, MAPK11, MAPK14,
MAPK8, MAPK9
46Link
n/aToxoplasmosisMAPK10, MAPK11, MAPK14,
MAPK8, MAPK9
46Link
n/aSalmonella infectionMAPK10, MAPK11, MAPK14,
MAPK8, MAPK9
46Link
n/aChagas diseaseMAPK10, MAPK11, MAPK14,
MAPK8, MAPK9
46Link
n/aHerpes simplex infectionCDK2, CSNK2A2, MAPK10,
MAPK8, MAPK9
5Link
n/aMeaslesCDK2, CSNK2A2, FYN, GSK3B7Link
n/aViral myocarditisABL1, ABL2, FYN1Link
Diabetes mellitusMAPK10, MAPK8, MAPK92Link
LeukemiaABL1, ABL21Link
Pfeiffer syndromeFGFR1, FGFR21Link
n/aPathogenic Escherichia coli infectionABL1, FYN1Link
n/aAmyotrophic lateral sclerosisMAPK11, MAPK1445Link
n/aLeishmaniasisMAPK11, MAPK1445Link
Jackson-Weiss syndromeFGFR1, FGFR21Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR21Link
Kallmann syndromeFGFR11Link
Gastric cancerFGFR21Link
Lung cancerCDK23Link
MelanomaFGFR11Link
Apert syndromeFGFR21Link
n/aMaturity onset diabetes of the youngBLK1Link
n/aBladder cancerDAPK11Link
Hypogonadotropic hypogonadismFGFR11Link
TrigonocephalyFGFR11Link
Osteoglophonic dysplasiaFGFR11Link
LADD syndromeFGFR21Link
Beare-Stevenson cutis gyrata syndromeFGFR21Link
n/aGlycogen storage diseasesPHKG21Link
n/aEpileptic encephalopathyMAPK102Link
n/aEarly infantile epileptic encephalopathyMAPK102Link
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
SCIDLCK2Link
n/aImmunodeficienciesLCK2Link
CraniosynostosisFGFR21Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR21Link
Bent bone dysplasia syndromeFGFR21Link
Crouzon syndromeFGFR21Link
n/aSaethre-Chotzen syndromeFGFR21Link
n/aBasal cell carcinomaGSK3B4Link
n/aPrion diseasesFYN1Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR21Link
ScaphocephalyFGFR21Link