Allelic Variants

There are no related allelic variants
Related diseases of KIF 3IPHA_G11 (PDB code: 3IPH, 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, MAPK11,
MAPK14, MAPK8, MAPK9
100Link
n/aEpithelial cell signaling in Helicobacter pylori infectionLYN, MAPK10, MAPK11, MAPK14,
MAPK8, MAPK9, SRC
89Link
n/aShigellosisABL1, MAPK10, MAPK11,
MAPK14, MAPK8, MAPK9, SRC
89Link
n/aTuberculosisMAPK10, MAPK11, MAPK14,
MAPK8, MAPK9, SRC
89Link
n/aHepatitis CGSK3B, MAPK10, MAPK11,
MAPK14, MAPK8, MAPK9
93Link
n/aHerpes simplex infectionCDC2, CDK2, CSNK2A2, MAPK10,
MAPK8, MAPK9
10Link
Prostate cancerCDK2, EPHB2, FGFR1, FGFR2,
GSK3B, PDPK1
19Link
n/aInfluenza AGSK3B, MAPK10, MAPK11,
MAPK14, MAPK8, MAPK9
93Link
n/aSalmonella infectionMAPK10, MAPK11, MAPK14,
MAPK8, MAPK9
87Link
n/aToxoplasmosisMAPK10, MAPK11, MAPK14,
MAPK8, MAPK9
87Link
n/aPertussisMAPK10, MAPK11, MAPK14,
MAPK8, MAPK9
87Link
n/aChagas diseaseMAPK10, MAPK11, MAPK14,
MAPK8, MAPK9
87Link
n/aMeaslesCDK2, CSNK2A2, FYN, GSK3B14Link
n/aViral myocarditisABL1, ABL2, FYN1Link
Diabetes mellitusMAPK10, MAPK8, MAPK92Link
n/aPathogenic Escherichia coli infectionABL1, FYN1Link
Jackson-Weiss syndromeFGFR1, FGFR22Link
LeukemiaABL1, ABL21Link
Pfeiffer syndromeFGFR1, FGFR22Link
n/aAmyotrophic lateral sclerosisMAPK11, MAPK1485Link
n/aLeishmaniasisMAPK11, MAPK1485Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR21Link
MelanomaFGFR12Link
Kallmann syndromeFGFR12Link
Gastric cancerFGFR21Link
Lung cancerCDK27Link
TrigonocephalyFGFR12Link
Apert syndromeFGFR21Link
n/aMaturity onset diabetes of the youngBLK1Link
n/aCocaine addictionCDK51Link
n/aBladder cancerDAPK11Link
Osteoglophonic dysplasiaFGFR12Link
Hypogonadotropic hypogonadismFGFR12Link
LADD syndromeFGFR21Link
Beare-Stevenson cutis gyrata syndromeFGFR21Link
n/aGlycogen storage diseasesPHKG21Link
n/aEpileptic encephalopathyMAPK101Link
n/aEarly infantile epileptic encephalopathyMAPK101Link
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
SCIDLCK3Link
n/aImmunodeficienciesLCK3Link
CraniosynostosisFGFR21Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR21Link
Bent bone dysplasia syndromeFGFR21Link
Crouzon syndromeFGFR21Link
n/aSaethre-Chotzen syndromeFGFR21Link
n/aBasal cell carcinomaGSK3B7Link
n/aPrion diseasesFYN1Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR21Link
ScaphocephalyFGFR21Link