Allelic Variants

There are no related allelic variants
Related diseases of KIF 2OU7A_ANP (PDB code: 2OU7, chain A)
Number of involved diseases in the family 50
Number of PLK1 related diseases 0
All kinase in this family  PLK1
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
Prostate cancerCDK2, CHEK2, FGFR1, FGFR2,
GSK3B, PDPK1
6Link
n/aMeaslesCDK2, EIF2AK2, GSK3B, IRAK43Link
n/aEpstein-Barr virus infectionCDK2, EIF2AK2, GSK3B, MAPK123Link
n/aInfluenza AEIF2AK2, GSK3B, IRAK4,
MAPK12
2Link
n/aHepatitis CEIF2AK2, GSK3B, MAPK122Link
Jackson-Weiss syndromeFGFR1, FGFR23Link
n/aPertussisIRAK4, MAPK121Link
n/aLeishmaniasisIRAK4, MAPK121Link
n/aChagas diseaseIRAK4, MAPK121Link
n/aToxoplasmosisIRAK4, MAPK121Link
n/aHerpes simplex infectionCDK2, EIF2AK22Link
Pfeiffer syndromeFGFR1, FGFR23Link
Lung cancerCDK2, PTK22Link
n/aTuberculosisIRAK4, MAPK121Link
Gastric cancerFGFR22Link
MelanomaFGFR11Link
TrigonocephalyFGFR11Link
Osteoglophonic dysplasiaFGFR11Link
Kallmann syndromeFGFR11Link
Breast cancerCHEK21Link
Hypogonadotropic hypogonadismFGFR11Link
Mental retardationCASK2Link
n/aFG syndromeCASK2Link
Li-Fraumeni syndromeCHEK21Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR22Link
n/aBladder cancerDAPK12Link
OsteosarcomaCHEK21Link
Beare-Stevenson cutis gyrata syndromeFGFR22Link
Apert syndromeFGFR22Link
n/aInvasive pneumococcal diseaseIRAK41Link
Hyperinsulinemic hypoglycemiaINSR3Link
Diabetes mellitusINSR3Link
IRAK4 deficiencyIRAK41Link
n/aAmyotrophic lateral sclerosisMAPK121Link
n/aAmoebiasisPTK22Link
n/aSalmonella infectionMAPK121Link
n/aShigellosisMAPK121Link
n/aEpithelial cell signaling in Helicobacter pylori infectionMAPK121Link
Rabson-Mendenhall syndromeINSR3Link
n/aLeprechaunismINSR3Link
CraniosynostosisFGFR22Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR22Link
Bent bone dysplasia syndromeFGFR22Link
Colon cancerAURKA3Link
Crouzon syndromeFGFR22Link
LADD syndromeFGFR22Link
n/aBasal cell carcinomaGSK3B2Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR22Link
ScaphocephalyFGFR22Link
n/aSaethre-Chotzen syndromeFGFR22Link