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

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Gene: ACRV1 ENSBTAG00000033384

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Description

acrosomal vesicle protein 1 [Source:VGNC Symbol;Acc:VGNC:25559]

Location

Primary_assembly 29: 29,060,611-29,067,118 reverse strand.

ARS-UCD1.3:CM008196.2

About this gene

This gene has 3 transcripts (splice variants), 91 orthologues and 7 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000047491.4	ACRV1-202	1160	273aa	ENSBTAP00000044695.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q32KR2	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,
ENSBTAT00000129781.1	ACRV1-201	1056	270aa	ENSBTAP00000074993.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000120213.1	ACRV1-203	968	209aa	ENSBTAP00000088568.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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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