Gene: Slc3a2 ENSRNOG00000018487

Description

solute carrier family 3 member 2 [Source:RGD Symbol;Acc:3073]

Gene Synonyms

4F2hc, Mdu1

Location

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants), 282 orthologues, 7 paralogues and is associated with 12 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000025196.5	Slc3a2-201	1979	566aa	ENSRNOP00000025196.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0H2UHQ0 A6HZS0	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,
ENSRNOT00000151218.1	Slc3a2-202	1916	545aa	ENSRNOP00000098826.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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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