Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6795
Gene name Gene Name - the full gene name approved by the HGNC.
Aurora kinase C
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
AURKC
Synonyms (NCBI Gene) Gene synonyms aliases
AIE2, AIK3, ARK3, AurC, HEL-S-90, SPGF5, STK13, aurora-C
Disease Acronyms (UniProt) Disease acronyms from UniProt database
SPGF5
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19q13.43
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the Aurora subfamily of serine/threonine protein kinases. The encoded protein is a chromosomal passenger protein that forms complexes with Aurora-B and inner centromere proteins and may play a role in organizing microtubules
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs74179426 ->C Conflicting-interpretations-of-pathogenicity 5 prime UTR variant, non coding transcript variant, intron variant
rs121908654 G>A Pathogenic Coding sequence variant, non coding transcript variant, missense variant
rs397515484 A>G Pathogenic Splice acceptor variant
rs397515619 C>- Pathogenic Frameshift variant, coding sequence variant, non coding transcript variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT812205 hsa-miR-125a-5p CLIP-seq
MIRT812206 hsa-miR-125b CLIP-seq
MIRT812207 hsa-miR-4319 CLIP-seq
MIRT812208 hsa-miR-4732-3p CLIP-seq
MIRT812209 hsa-miR-4768-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000793 Component Condensed chromosome IDA 15670791
GO:0004672 Function Protein kinase activity IDA 15670791
GO:0004712 Function Protein serine/threonine/tyrosine kinase activity TAS 19774610
GO:0005515 Function Protein binding IPI 21988832, 27332895, 32296183
GO:0005524 Function ATP binding IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
603495 11391 ENSG00000105146
Protein
UniProt ID Q9UQB9
Protein name Aurora kinase C (EC 2.7.11.1) (Aurora 3) (Aurora/IPL1-related kinase 3) (ARK-3) (Aurora-related kinase 3) (Aurora/IPL1/Eg2 protein 2) (Serine/threonine-protein kinase 13) (Serine/threonine-protein kinase aurora-C)
Protein function Serine/threonine-protein kinase component of the chromosomal passenger complex (CPC), a complex that acts as a key regulator of mitosis. The CPC complex has essential functions at the centromere in ensuring correct chromosome alignment and segre
PDB 6GR8 , 6GR9 , 9ESA
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00069 Pkinase 43 293 Protein kinase domain Domain
Tissue specificity TISSUE SPECIFICITY: Isoform 1 and isoform 2 are expressed in testis. Elevated expression levels were seen only in a subset of cancer cell lines such as Hep-G2, Huh-7 and HeLa. Expression is maximum at M phase. {ECO:0000269|PubMed:15670791}.
Sequence
Sequence length 309
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Infertility associated with multi-tailed spermatozoa and excessive dna Male Infertility with Large-Headed, Multiflagellar, Polyploid Spermatozoa rs397515619, rs121908654, rs397515484 21733974, 17435757
Lung carcinoma Squamous cell carcinoma of lung rs1805076, rs121909071, rs121913530, rs112445441, rs121913529, rs121913535, rs121913297, rs121913279, rs104886003, rs397516975, rs11554290, rs121913364, rs121913351, rs121913369, rs121913355
View all (44 more)
Lung adenocarcinoma Adenocarcinoma of lung (disorder) rs28934576, rs121913530, rs397516975, rs587776805, rs121913469, rs121913364, rs121913351, rs121913366, rs397516896, rs397516977, rs397516981, rs397517127, rs121913344, rs727504233, rs121913370
View all (5 more)
Male infertility Male infertility due to large-headed multiflagellar polyploid spermatozoa rs554675432, rs9332971, rs397507505, rs797045116, rs748618094, rs781431741, rs1555979575, rs377581367
Unknown
Disease term Disease name Evidence References Source
Spermatogenic Failure spermatogenic failure 5 GenCC
Associations from Text Mining
Disease Name Relationship Type References
Breast Neoplasms Associate 25994570
Carcinogenesis Associate 25990457
Fetal Growth Retardation Inhibit 32452402
Glioblastoma Associate 34465813
Infertility Associate 25219909, 26341096
Infertility Male Associate 24484996, 25219909, 30594972
Klinefelter Syndrome Associate 25219909
Male Infertility with Large Headed Multiflagellar Polyploid Spermatozoa Associate 24484996
Megalencephaly Associate 23273756, 25755131
Neoplasms Associate 10066797, 21762492, 22283874, 24603334, 25990457, 25994570