Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
9212
Gene name Gene Name - the full gene name approved by the HGNC.
Aurora kinase B
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
AURKB
Synonyms (NCBI Gene) Gene synonyms aliases
AIK2, AIM-1, AIM1, ARK-2, ARK2, AurB, IPL1, PPP1R48, STK-1, STK12, STK5, aurkb-sv1, aurkb-sv2
Chromosome Chromosome number
17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
17p13.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the aurora kinase subfamily of serine/threonine kinases. The genes encoding the other two members of this subfamily are located on chromosomes 19 and 20. These kinases participate in the regulation of alignment and segregatio
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs1597343914 G>A Likely-pathogenic Missense variant, coding sequence variant, non coding transcript variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT004742 hsa-miR-16-5p Microarray, qRT-PCR 19738602
MIRT004742 hsa-miR-16-5p Microarray, qRT-PCR 19738602
MIRT004742 hsa-miR-16-5p Microarray, qRT-PCR 19738602
MIRT000120 hsa-miR-24-3p Luciferase reporter assay, Microarray, qRT-PCR, Western blot 19748357
MIRT000120 hsa-miR-24-3p Luciferase reporter assay, Microarray, qRT-PCR, Western blot 19748357
Transcription factors
Transcription factor Regulation Reference
E2F1 Unknown 15033491
E2F4 Unknown 15033491
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000122 Process Negative regulation of transcription by RNA polymerase II IDA 20959462
GO:0000166 Function Nucleotide binding IEA
GO:0000278 Process Mitotic cell cycle NAS 17956729
GO:0000281 Process Mitotic cytokinesis NAS 17956729
GO:0000775 Component Chromosome, centromeric region IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
604970 11390 ENSG00000178999
Protein
UniProt ID Q96GD4
Protein name Aurora kinase B (EC 2.7.11.1) (Aurora 1) (Aurora- and IPL1-like midbody-associated protein 1) (AIM-1) (Aurora/IPL1-related kinase 2) (ARK-2) (Aurora-related kinase 2) (STK-1) (Serine/threonine-protein kinase 12) (Serine/threonine-protein kinase 5) (Serine
Protein function Serine/threonine-protein kinase component of the chromosomal passenger complex (CPC), a complex that acts as a key regulator of mitosis (PubMed:11516652, PubMed:12925766, PubMed:14610074, PubMed:14722118, PubMed:29449677). The CPC complex has es
PDB 4AF3
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00069 Pkinase 77 327 Protein kinase domain Domain
Tissue specificity TISSUE SPECIFICITY: High level expression seen in the thymus. It is also expressed in the spleen, lung, testis, colon, placenta and fetal liver. Expressed during S and G2/M phase and expression is up-regulated in cancer cells during M phase. {ECO:0000269|
Sequence
Sequence length 344
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Polycomb repressive complex
Cell cycle
  Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal
APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1
Separation of Sister Chromatids
Resolution of Sister Chromatid Cohesion
SUMOylation of DNA replication proteins
RHO GTPases Activate Formins
Regulation of TP53 Activity through Phosphorylation
Mitotic Prometaphase
EML4 and NUDC in mitotic spindle formation
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Anxiety Disorder Anxiety disorders N/A N/A GWAS
Neuroticism Neuroticism N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
2 Hydroxyglutaricaciduria Associate 22971244
Adenocarcinoma of Lung Associate 27610375, 33612479, 33684161, 34039308, 35354488
Adenocarcinoma of Lung Stimulate 34397793
Adenomatous Polyps Associate 26423403
Adrenocortical Carcinoma Associate 30413320
Anemia Refractory Stimulate 22419576
Aneuploidy Associate 24782314, 29707994, 31967936, 33293370, 35044816
Astrocytoma Associate 22971244, 27106762
Barrett Esophagus Associate 21470402
Breast Neoplasms Associate 21707964, 24324792, 25755770, 25885472, 29196757, 31083605, 31142743, 34736137, 35456460, 36281185, 40710353