Allelic Variants

There are no related allelic variants
Related diseases of KIF 2BMCA_MPY (PDB code: 2BMC, chain A)
Number of involved diseases in the family 107
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/aEpstein-Barr virus infectionCDC2, CDK2, CSNK2A1,
CSNK2A2, GSK3B, JAK1, JAK3,
MAP2K4, MAPK10, MAPK8, RIPK1
21Link
n/aMeaslesCDK2, CDK4, CSNK2A1,
CSNK2A2, GSK3B, IRAK4, JAK1,
JAK2, JAK3, PRKCQ
37Link
n/aHerpes simplex infectionCDC2, CDK2, CSNK2A1,
CSNK2A2, JAK1, JAK2, MAPK10,
MAPK8
15Link
n/aInfluenza AGSK3B, IRAK4, JAK1, JAK2,
MAP2K4, MAPK10, MAPK8, RAF1
9Link
n/aHepatitis CEGFR, GSK3B, JAK1, MAPK10,
MAPK8, RAF1, RIPK1
10Link
n/aTuberculosisCAMK2A, IRAK4, JAK1, JAK2,
MAPK10, MAPK8, RAF1
3Link
Prostate cancerCDK2, EGFR, FGFR1, FGFR2,
GSK3B, PDPK1, RAF1
36Link
LeukemiaABL1, ABL2, CDK4, JAK2,
RAF1, RPS6KB1
26Link
Lung cancerALK, CDK2, CDK4, EGFR, PTK232Link
n/aToxoplasmosisIRAK4, JAK1, JAK2, MAPK10,
MAPK8
2Link
MelanomaCDK4, EGFR, FGFR1, RAF129Link
n/aAlcoholismCAMKK1, CAMKK2, NTRK2, RAF12Link
Diabetes mellitusMAPK10, MAPK8, PRKCD, PRKCZ6Link
n/aChagas diseaseIRAK4, MAP2K4, MAPK10, MAPK81Link
NeuroblastomaALK, NTRK1, NTRK2, NTRK33Link
n/aEpithelial cell signaling in Helicobacter pylori infectionEGFR, MAP2K4, MAPK10, MAPK83Link
n/aPertussisIRAK4, MAPK10, MAPK81Link
n/aSalmonella infectionMAPK10, MAPK8, PKN21Link
n/aCardiomyopathyMYLK2, PRKAA1, PRKAA21Link
n/aLeishmaniasisIRAK4, JAK1, JAK22Link
n/aImmunodeficienciesJAK3, LCK, ZAP7011Link
n/aCervical cancerCDK4, EGFR, FGFR323Link
n/aShigellosisABL1, MAPK10, MAPK84Link
Gastric cancerEGFR, FGFR23Link
Pfeiffer syndromeFGFR1, FGFR26Link
Jackson-Weiss syndromeFGFR1, FGFR26Link
n/aViral myocarditisABL1, ABL24Link
n/aThyroid cancerNTRK1, RET3Link
n/aBladder cancerEGFR, FGFR33Link
SCIDJAK3, LCK11Link
n/aMedullary thyroid carcinomaNTRK1, RET3Link
n/aGliomaCDK4, EGFR23Link
LADD syndromeFGFR2, FGFR32Link
Crouzon syndromeFGFR2, FGFR32Link
Beare-Stevenson cutis gyrata syndromeFGFR21Link
TrigonocephalyFGFR16Link
Bent bone dysplasia syndromeFGFR21Link
n/aPathogenic Escherichia coli infectionABL14Link
Craniofacial-skeletal-dermatologic dysplasiaFGFR21Link
Kallmann syndromeFGFR16Link
Apert syndromeFGFR21Link
n/aAntley-Bixler syndrome without genital anomalies or disordered steroidogenesisFGFR21Link
CraniosynostosisFGFR21Link
Colon cancerAURKA37Link
Osteoglophonic dysplasiaFGFR16Link
n/aSaethre-Chotzen syndromeFGFR21Link
n/aEsophageal cancerEGFR2Link
n/aOral cancerEGFR2Link
n/aAgammaglobulinemia and isolated hormone deficiencyBTK1Link
n/aMalignant melanomaCDK421Link
n/aCocaine addictionCDK52Link
n/aChoriocarcinomaEGFR2Link
n/aLaryngeal cancerEGFR2Link
n/aMaturity onset diabetes of the youngBLK1Link
Hypogonadotropic hypogonadismFGFR16Link
n/aAgammaglobulinemiasBTK1Link
Adenocarcinoma of lungEGFR2Link
AgammaglobulinemiaBTK1Link
n/aPituitary DwarfismBTK1Link
Colorectal cancerFGFR32Link
ScaphocephalyFGFR21Link
n/aCirrhosis due to liver phosphorylase kinase deficiencyPHKG21Link
Glycogen storage diseasePHKG21Link
n/aType I diabetes mellitusPRKCQ2Link
n/aAmoebiasisPTK21Link
n/aGlycogen storage diseasesPHKG21Link
n/aObesityNTRK21Link
n/aEpileptic encephalopathyMAPK101Link
n/aFamilial thoracic aortic aneurysm and dissectionMYLK1Link
n/aAortic aneurysmMYLK1Link
n/aInsensitivity to painNTRK12Link
LEOPARD syndromeRAF11Link
Noonan syndromeRAF11Link
Renal agenesisRET2Link
Venous malformationsTEK2Link
n/aRheumatoid arthritisTEK2Link
Selective T-cell defectZAP701Link
PheochromocytomaRET2Link
Multiple endocrine neoplasiaRET2Link
n/aRenal agenesis and Renal adysplasiaRET2Link
Hirschsprung diseaseRET2Link
n/aCongenital central hypoventilation syndromeRET2Link
Central hypoventilation syndromeRET2Link
n/aEarly infantile epileptic encephalopathyMAPK101Link
ThrombocythemiaJAK22Link
n/aMuenke syndromeFGFR32Link
n/aNevusFGFR32Link
n/aSpermatocytic seminomaFGFR32Link
n/aThanatophoric dysplasiaFGFR32Link
n/aHypochondroplasiaFGFR32Link
n/aAchondroplasiaFGFR32Link
n/aScaphocephaly and Axenfeld-Rieger anomalyFGFR21Link
n/aMultiple myelomaFGFR32Link
n/aFGFR3-related short limb skeletal dysplasiasFGFR32Link
n/aCATSHL syndromeFGFR32Link
n/aCancer progression/metastasisFGFR41Link
n/aCongenital stationary night blindnessGRK11Link
Polycythemia veraJAK22Link
n/aBudd-Chiari syndromeJAK22Link
MyelofibrosisJAK22Link
n/aMyeloproliferative disorderJAK22Link
Lymphoproliferative syndromeITK5Link
IRAK4 deficiencyIRAK41Link
n/aOguchi diseaseGRK11Link
n/aBasal cell carcinomaGSK3B7Link
n/aEndocrine-cerebroosteodysplasiaICK1Link
n/aInvasive pneumococcal diseaseIRAK41Link