Gene: Aurkc ENSRNOG00000015825

Description

aurora kinase C [Source:RGD Symbol;Acc:1309573]

Gene Synonyms

LOC103691033, LOC292554

Location

Primary_assembly 1: 75,876,773-75,897,426 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 5 transcripts (splice variants), 99 orthologues, 2 paralogues and is associated with 4 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000021245.9	Aurkc-201	1314	329aa	ENSRNOP00000021248.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4AD76	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS ALT2,
ENSRNOT00000151126.1	Aurkc-205	1338	320aa	ENSRNOP00000103752.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000137845.1	Aurkc-204	1300	282aa	ENSRNOP00000108887.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000119494.2	Aurkc-203	1251	308aa	ENSRNOP00000078675.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6G3L3	-
ENSRNOT00000119286.2	Aurkc-202	1221	298aa	ENSRNOP00000088690.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GHC0	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P2,