Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
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  - Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
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ID History
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Gene: BMERB1 ENSBTAG00000011692

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Description

bMERB domain containing 1 [Source:VGNC Symbol;Acc:VGNC:52685]

Gene Synonyms

C25H16ORF45

Location

Primary_assembly 25: 13,881,271-14,026,628 forward strand.

ARS-UCD2.0:CM008192.2

About this gene

This gene has 3 transcripts (splice variants) and 205 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000071578.3	BMERB1-201	2468	202aa	ENSBTAP00000058245.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LHK9	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,
ENSBTAT00000015524.7	BMERB1-202	4315	185aa	ENSBTAP00000015524.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0JN56	-
ENSBTAT00000128795.2	BMERB1-203	2062	189aa	ENSBTAP00000082456.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SFR9	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be 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 P2,

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Summary

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