AURKA (Aurora Kinase A) Gene

A serine/threonine kinase critical for mitotic spindle assembly and chromosome segregation; frequently amplified in cancer.

Gene Information Card

Symbol AURKA
Full Name aurora kinase A
Gene Type protein-coding
Chromosomal Location 20q13.2
NCBI Gene ID 6790 ncbi.nlm.nih.gov/gene/6790
Ensembl ID ENSG00000087586
UniProt ID O14965
OMIM ID 603072
HGNC ID 11393
Aliases STK15, BTAK, AIK, ARK1, AURA, PPP1R47

Description

AURKA encodes a cell cycle-regulated serine/threonine kinase that localizes to the centrosome and spindle poles during mitosis. It is essential for centrosome maturation, spindle assembly, and chromosome segregation. Overexpression and gene amplification of AURKA are oncogenic drivers in multiple human cancers, leading to aneuploidy and genomic instability.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Breast cancer Amplification and overexpression of AURKA lead to centrosome amplification and aneuploidy, promoting tumorigenesis. PMID: 15688063; COSMIC; ClinVar
Ovarian cancer AURKA amplification (20q13.2) is recurrent in high-grade serous ovarian carcinoma, associated with poor prognosis. PMID: 21720365; COSMIC
Colorectal cancer AURKA overexpression correlates with chromosomal instability and poor survival. PMID: 12506203; COSMIC
Neuroblastoma AURKA stabilizes MYCN protein, contributing to oncogenic signaling. PMID: 19252505; ClinVar

Expression Profile

Tissue Expression
Tissue nTPM level
Bone marrow 15.2 Medium
Testis 12.8 Medium
Lymph node 10.5 Medium
Colon 8.3 Low
Breast 6.1 Low
Ovary 5.9 Low
Cell Line Expression
Cell Line nTPM Notes
HeLa 18.4 Cervical adenocarcinoma; high expression
MCF7 14.2 Breast cancer; moderate expression
A549 11.7 Lung carcinoma; moderate expression
K562 9.3 Chronic myeloid leukemia; low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.91G>A (p.Glu31Lys) Missense <0.1% Unknown functional impact; rare in COSMIC
c.169A>G (p.Ile57Val) Missense <0.1% Reported in colorectal cancer; functional significance unclear
c.911T>C (p.Phe304Ser) Missense <0.1% Kinase domain; potential loss-of-function in vitro
Amplification Copy number gain ~10-20% in breast/ovarian Gain-of-function; drives oncogenesis
Mutation functional classification

Loss of Function (LOF)

Rare missense variants in the kinase domain (e.g., p.Phe304Ser) reduce catalytic activity in vitro, but no clear loss-of-function disease phenotype is established.

Gain of Function (GOF)

Gene amplification and overexpression are the primary gain-of-function mechanisms, leading to increased kinase activity, centrosome amplification, and aneuploidy.

Dominant Negative (DN)

No well-characterized dominant-negative mutations reported in human disease.

Pathways

Cell Cycle
Mitotic (Reactome R-HSA-69278)
Aurora A signaling (Reactome R-HSA-8854518)
PLK1 signaling events (Reactome R-HSA-1566948)
G2/M DNA damage checkpoint (Reactome R-HSA-69481)

Protein Summary

Aurora kinase A (AURKA) is a 403-amino-acid serine/threonine kinase with an N-terminal regulatory domain and a C-terminal catalytic domain. It is activated by autophosphorylation at Thr288 and localized to centrosomes and spindle poles during mitosis. AURKA phosphorylates substrates including TPX2, CEP192, and BORA to promote centrosome maturation, spindle assembly, and mitotic entry. Overexpression leads to centrosome amplification, multipolar spindles, and aneuploidy, making it a target for cancer therapy (e.g., alisertib).

Related Products

Product name Cat.No. Species Gene ID
AURKA Knockout HEK293 Cell Line EDJ-KQ50666 Human 6790 Details Get a Quote
AURKA Knockout HeLa Cell Line EDJ-KQ54585 Human 6790 Details Get a Quote
AURKA Knockout A-549 Cell Line EDJ-KQ63069 Human 6790 Details Get a Quote
AURKA Knockout HCT 116 Cell Line EDJ-KQ71545 Human 6790 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
Contact Us
*
*
*
*
How did you hear about us: