Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
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Ontologies
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
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ID History
- Gene history

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Gene: Vom2r57 ENSRNOG00000039136

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Description

vomeronasal 2 receptor, 57 [Source:RGD Symbol;Acc:1562007]

Gene Synonyms

LOC299683, RGD1562007

Location

Primary_assembly 7: 15,741,942-15,759,868 reverse strand.

mRatBN7.2:CM026980.1

About this gene

This gene has 1 transcript (splice variant), 101 orthologues and 98 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000049266.6	Vom2r57-201	2586	861aa	ENSRNOP00000041673.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZME2	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,

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Summary

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