Allelic Variants

There are no related allelic variants
Related diseases of KIF 2NP8A_CC3 (PDB code: 2NP8, chain A)
Number of involved diseases in the family 54
Number of AURKA related diseases 1
All kinase in this family  AURKA
Allelic
Variants
Disease Description Involved kinases
(This family)
Inhibitor of
Involved Kinases
Search
Disease
n/aHepatitis CBRAF, EGFR, MAPK10, MAPK813Link
n/aHerpes simplex infectionCSNK2A1, JAK2, MAPK10, MAPK812Link
n/aTuberculosisJAK2, MAPK10, MAPK87Link
Prostate cancerBRAF, EGFR, FGFR19Link
n/aInfluenza AJAK2, MAPK10, MAPK87Link
MelanomaBRAF, EGFR, FGFR19Link
Lung cancerBRAF, EGFR, PTK28Link
n/aEpstein-Barr virus infectionCSNK2A1, MAPK10, MAPK811Link
LeukemiaABL1, BRAF, JAK25Link
n/aEpithelial cell signaling in Helicobacter pylori infectionEGFR, MAPK10, MAPK812Link
n/aToxoplasmosisJAK2, MAPK10, MAPK87Link
n/aShigellosisABL1, MAPK10, MAPK89Link
Adenocarcinoma of lungBRAF, EGFR7Link
n/aSalmonella infectionMAPK10, MAPK86Link
Diabetes mellitusMAPK10, MAPK86Link
n/aPertussisMAPK10, MAPK86Link
n/aMeaslesCSNK2A1, JAK26Link
n/aChagas diseaseMAPK10, MAPK86Link
Noonan syndromeBRAF1Link
n/aOral cancerEGFR6Link
n/aPathogenic Escherichia coli infectionABL13Link
LEOPARD syndromeBRAF1Link
n/aNoonan syndrome and related disordersBRAF1Link
n/aThyroid cancerBRAF1Link
n/aMalignant melanomaBRAF1Link
n/aAlcoholismBRAF1Link
Colon cancerAURKA4Link
n/aEsophageal cancerEGFR6Link
Colorectal cancerBRAF1Link
Cardiofaciocutaneous syndromeBRAF1Link
n/aViral myocarditisABL13Link
n/aCervical cancerEGFR6Link
Gastric cancerEGFR6Link
n/aMyeloproliferative disorderJAK21Link
MyelofibrosisJAK21Link
n/aBudd-Chiari syndromeJAK21Link
ThrombocythemiaJAK21Link
n/aImmunodeficienciesLCK1Link
n/aAmoebiasisPTK21Link
n/aEpileptic encephalopathyMAPK105Link
n/aEarly infantile epileptic encephalopathyMAPK105Link
SCIDLCK1Link
n/aLeishmaniasisJAK21Link
Polycythemia veraJAK21Link
n/aLaryngeal cancerEGFR6Link
n/aGliomaEGFR6Link
n/aChoriocarcinomaEGFR6Link
n/aBladder cancerEGFR6Link
Hypogonadotropic hypogonadismFGFR12Link
Osteoglophonic dysplasiaFGFR12Link
Pfeiffer syndromeFGFR12Link
Kallmann syndromeFGFR12Link
Jackson-Weiss syndromeFGFR12Link
TrigonocephalyFGFR12Link