Gene: brinp2 ENSDARG00000014302

Description

bone morphotic protein/retinoic acid inducible neural-specific 2 [Source:NCBI gene (formerly Entrezgene);Acc:561009]

Location

GRCz11:CM002886.2

About this gene

This gene has 2 transcripts (splice variants), 209 orthologues, 4 paralogues and is associated with 2 phenotypes.

Transcripts

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000133224.2	brinp2-202	2325	774aa	ENSDARP00000112914.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSDART00000056671.6	brinp2-201	3117	776aa	ENSDARP00000056670.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8M1P6S6	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,

Summary