Gene: Slc5a6 ENSRNOG00000057628

Description

solute carrier family 5 member 6 [Source:RGD Symbol;Acc:69648]

Gene Synonyms

SMVT

Location

GRCr8:CM070396.1

About this gene

This gene has 1 transcript (splice variant), 271 orthologues, 13 paralogues and is associated with 4 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000082623.3	Slc5a6-201	3234	634aa	ENSRNOP00000075361.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B4F760 O70247	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,

Strains

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.