Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: BRINP2 ENSSSCG00000015515

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Description

BMP/retinoic acid inducible neural specific 2 [Source:VGNC Symbol;Acc:VGNC:85882]

Location

Primary_assembly 9: 118,975,719-119,095,336 forward strand.

Sscrofa11.1:CM000820.5

About this gene

This gene has 1 transcript (splice variant), 354 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000064518.3	BRINP2-201	4072	787aa	ENSSSCP00000038439.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1ZKY8 F1S6Z1	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 P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,

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Summary

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