Gene: Tsc22d2 ENSRNOG00000038044

Description

TSC22 domain family, member 2 [Source:RGD Symbol;Acc:1593169]

Gene Synonyms

LOC499624

Location

GRCr8:CM070392.1

About this gene

This gene has 2 transcripts (splice variants), 233 orthologues, 4 paralogues and is associated with 2 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000015119.8	Tsc22d2-201	4797	768aa	ENSRNOP00000062527.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZDW3	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,
ENSRNOT00000088139.3	Tsc22d2-202	4725	744aa	ENSRNOP00000073091.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K4L6 A6JVI5	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,

Strains

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