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 PRKG2 related diseases 0
All kinase in this family  PRKG2
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