Gene: Sh3pxd2b ENSRNOG00000004063

Description

SH3 and PX domains 2B [Source:RGD Symbol;Acc:1309926]

Gene Synonyms

LOC303021, RGD1309926

Location

GRCr8:CM070400.1

About this gene

This gene has 2 transcripts (splice variants), 204 orthologues, 3 paralogues and is associated with 13 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000073675.5	Sh3pxd2b-202	7442	935aa	ENSRNOP00000067367.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M0RCP2	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 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,
ENSRNOT00000005478.7	Sh3pxd2b-201	7358	907aa	ENSRNOP00000005478.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZAF9	APPRIS P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform as 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 P4,

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