Gene: Slc7a2 ENSRNOG00000011016

Description

solute carrier family 7 member 2 [Source:RGD Symbol;Acc:68387]

Gene Synonyms

CAT-2, Cat2, Cat2a, Cat2b, RCAT2

Location

GRCr8:CM070406.1

About this gene

This gene has 2 transcripts (splice variants), 243 orthologues, 17 paralogues and is associated with 3 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000014809.7	Slc7a2-201	2500	658aa	ENSRNOP00000014809.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B5D5N9-2	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 ALT1: 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 is conserved in at least 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 ALT1,
ENSRNOT00000015127.7	Slc7a2-202	2497	657aa	ENSRNOP00000015127.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B5D5N9-1	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,

Summary