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

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Gene: BRINP2 ENSG00000198797

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Description

bone morphogenetic protein/retinoic acid inducible neural-specific 2 [Source:HGNC Symbol;Acc:13746]

Gene Synonyms

DBCCR1L2, FAM5B, KIAA1747, RP5-1026E2.1

Location

Chromosome 1: 177,140,633-177,251,558 forward strand.

GRCh37:CM000663.1

About this gene

This gene has 3 transcripts (splice variants), 354 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000361539.4	BRINP2-001	3558	783aa	ENSP00000354481.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS1320	Q9C0B6	NM_021165.2	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, A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic,
ENST00000478325.1	BRINP2-002	2494	No protein	-	Gene/transcript that doesn't contain an open reading frame (ORF).Processed transcript		-	-	-
ENST00000460161.1	BRINP2-003	373	No protein	-	Gene/transcript that doesn't contain an open reading frame (ORF).Processed transcript		-	-	-

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Summary

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