Gene: Shd ENSRNOG00000049983

Description

src homology 2 domain-containing transforming protein D [Source:RGD Symbol;Acc:1590885]

Gene Synonyms

LOC316507

Location

mRatBN7.2:CM026982.1

About this gene

This gene has 2 transcripts (splice variants), 267 orthologues, 3 paralogues and is associated with 2 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000074767.3	Shd-201	1468	344aa	ENSRNOP00000065655.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M0R864	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,
ENSRNOT00000106114.1	Shd-202	2339	343aa	ENSRNOP00000089807.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B0BN15	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,

Summary