Gene: Slc16a8 ENSRNOG00000012090

Description

solute carrier family 16 member 8 [Source:RGD Symbol;Acc:69282]

Gene Synonyms

MCT 3, Mct3

Location

GRCr8:CM070397.1

About this gene

This gene has 2 transcripts (splice variants), 169 orthologues, 12 paralogues and is associated with 1 phenotype.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000141346.1	Slc16a8-202	1951	528aa	ENSRNOP00000112680.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000016247.5	Slc16a8-201	1829	490aa	ENSRNOP00000016248.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	O70461	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,

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