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: ERO1B ENSBTAG00000034633

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Description

endoplasmic reticulum oxidoreductase 1 beta [Source:VGNC Symbol;Acc:VGNC:28595]

Location

Primary_assembly 28: 8,900,531-9,000,395 reverse strand.

ARS-UCD2.0:CM008195.2

About this gene

This gene has 6 transcripts (splice variants), 204 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000109427.1	ERO1B-205	2125	488aa	ENSBTAP00000079572.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9S6N7	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,
ENSBTAT00000120029.1	ERO1B-202	2655	484aa	ENSBTAP00000101964.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TTL1	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,
ENSBTAT00000104245.1	ERO1B-201	2594	460aa	ENSBTAP00000100509.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TTU8	-
ENSBTAT00000001099.7	ERO1B-203	1901	471aa	ENSBTAP00000001099.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MW08	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,
ENSBTAT00000118144.1	ERO1B-206	1819	452aa	ENSBTAP00000082111.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9S9X8	-
ENSBTAT00000100639.1	ERO1B-204	1749	429aa	ENSBTAP00000084133.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SFI5	-

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Summary

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