Gene: Msh6 ENSRNOG00000016134

Description

mutS homolog 6 [Source:RGD Symbol;Acc:2322311]

Gene Synonyms

LOC100360342

Location

mRatBN7.2:CM026979.1

About this gene

This gene has 2 transcripts (splice variants), 201 orthologues, 3 paralogues and is associated with 53 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000093689.2	Msh6-202	4259	1361aa	ENSRNOP00000076177.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A1W2Q695	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 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,
ENSRNOT00000021923.8	Msh6-201	4816	1336aa	ENSRNOP00000021923.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A0U9	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,