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
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Vom1r105 ENSRNOG00000049645

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Description

vomeronasal 1 receptor 105 [Source:RGD Symbol;Acc:708382]

Gene Synonyms

Vmn1r51, Vn1, Vnr1

Location

Primary_assembly 4: 124,325,357-124,327,068 forward strand.

GRCr8:CM070394.1

About this gene

This gene has 1 transcript (splice variant), 218 orthologues and 88 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000088379.3	Vom1r105-201	975	324aa	ENSRNOP00000072684.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K3L2	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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