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

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Gene: BRINP1 ENSBTAG00000015936

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Description

BMP/retinoic acid inducible neural specific 1 [Source:VGNC Symbol;Acc:VGNC:26567]

Location

Primary_assembly 8: 108,637,081-108,834,345 reverse strand.

ARS-UCD2.0:CM008175.2

About this gene

This gene has 2 transcripts (splice variants), 204 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000021192.4	BRINP1-201	3092	761aa	ENSBTAP00000021192.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1N6R0	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,
ENSBTAT00000043723.2	BRINP1-202	2095	244aa	ENSBTAP00000041273.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MLS6	-

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Summary

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