Allelic Variants

There are no related allelic variants
Related diseases of KIF 1FQ1B_ATP (PDB code: 1FQ1, chain B)
Number of involved diseases in the family 66
Number of CDK2 related diseases 5
All kinase in this family  CDK2
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
Prostate cancerAKT2, CDK2, CHEK2, FGFR1,
FGFR2, GSK3B, MAP2K1, PDPK1
7Link
n/aInfluenza AAKT2, EIF2AK2, GSK3B, IRAK4,
MAP2K1, MAPK10, MAPK12
4Link
n/aEpstein-Barr virus infectionAKT2, CDK2, CSNK2A1,
EIF2AK2, GSK3B, MAPK10,
MAPK12
3Link
n/aMeaslesAKT2, CDK2, CSNK2A1,
EIF2AK2, GSK3B, IRAK4
3Link
n/aHepatitis CAKT2, EIF2AK2, GSK3B,
MAPK10, MAPK12
2Link
n/aShigellosisABL1, MAPK10, MAPK12, ROCK1,
SRC
6Link
n/aTuberculosisAKT2, IRAK4, MAPK10, MAPK12,
SRC
4Link
n/aHerpes simplex infectionCDK2, CSNK2A1, EIF2AK2,
MAPK10
2Link
LeukemiaABL1, AKT2, MAP2K1, PIM16Link
n/aChagas diseaseAKT2, IRAK4, MAPK10, MAPK121Link
MelanomaAKT2, FGFR1, MAP2K1, MET5Link
n/aEpithelial cell signaling in Helicobacter pylori infectionMAPK10, MAPK12, MET, SRC5Link
n/aToxoplasmosisAKT2, IRAK4, MAPK10, MAPK121Link
n/aPertussisIRAK4, MAPK10, MAPK121Link
n/aSalmonella infectionMAPK10, MAPK12, ROCK11Link
Diabetes mellitusAKT2, MAPK101Link
n/aPathogenic Escherichia coli infectionABL1, ROCK13Link
Pfeiffer syndromeFGFR1, FGFR23Link
Jackson-Weiss syndromeFGFR1, FGFR23Link
Colon cancerAURKA, SRC6Link
Lung cancerAKT2, CDK22Link
Gastric cancerFGFR2, MET3Link
n/aLeishmaniasisIRAK4, MAPK121Link
n/aImmunodeficienciesLCK, ZAP701Link
ScaphocephalyFGFR22Link
n/aAlcoholismMAP2K14Link
Cardiofaciocutaneous syndromeMAP2K14Link
n/aEarly infantile epileptic encephalopathyMAPK101Link
n/aPrion diseasesMAP2K14Link
n/aNoonan syndrome and related disordersMAP2K14Link
n/aFG syndromeCASK2Link
SCIDLCK1Link
Hypoinsulinemic hypoglycemiaAKT21Link
n/aEpileptic encephalopathyMAPK101Link
n/aAmyotrophic lateral sclerosisMAPK121Link
n/aViral myocarditisABL12Link
Hepatocellular carcinomaMET1Link
Selective T-cell defectZAP701Link
Ovarian cancerAKT21Link
n/aFamilial partial lipodystrophyAKT21Link
Renal cell carcinomaMET1Link
n/aCholangiocarcinomaMET1Link
n/aMalariaMET1Link
n/aAutism suseptibilityMET1Link
Mental retardationCASK2Link
n/aBasal cell carcinomaGSK3B2Link
Beare-Stevenson cutis gyrata syndromeFGFR22Link
Apert syndromeFGFR22Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR22Link
Bent bone dysplasia syndromeFGFR22Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR22Link
n/aSaethre-Chotzen syndromeFGFR22Link
LADD syndromeFGFR22Link
Crouzon syndromeFGFR22Link
CraniosynostosisFGFR22Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR22Link
n/aInvasive pneumococcal diseaseIRAK41Link
OsteosarcomaCHEK21Link
Breast cancerCHEK21Link
Li-Fraumeni syndromeCHEK21Link
n/aBladder cancerDAPK12Link
Hypogonadotropic hypogonadismFGFR11Link
Kallmann syndromeFGFR11Link
IRAK4 deficiencyIRAK41Link
TrigonocephalyFGFR11Link
Osteoglophonic dysplasiaFGFR11Link