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

Configure this page

Share this page

Bookmark this page

.

Gene: Vmn2r58 ENSMUSG00000090383

.

Description

vomeronasal 2, receptor 58 [Source:MGI Symbol;Acc:MGI:3647877]

Gene Synonyms

EG628422

Location

Chromosome 7: 41,485,238-41,522,136 reverse strand.

GRCm39:CM001000.3

About this gene

This gene has 7 transcripts (splice variants), 119 orthologues and 128 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000171671.3	Vmn2r58-201	3698	862aa	ENSMUSP00000126966.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS52212	K7N6V2	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic, 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, TSL 5: A transcript where no single transcript supports the model structure. The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users, based on the type and quality of the alignments used to annotate the transcript. TSL:5,
ENSMUST00000233081.2	Vmn2r58-203	3574	517aa	ENSMUSP00000156803.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A3B2WD23	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENSMUST00000233147.2	Vmn2r58-204	4085	72aa	ENSMUSP00000156405.2	Nonsense mediated decay		A0A3B2W3G0	-
ENSMUST00000233389.2	Vmn2r58-206	3957	91aa	ENSMUSP00000156834.2	Nonsense mediated decay		A0A3B2WBE4	-
ENSMUST00000233177.2	Vmn2r58-205	3874	524aa	ENSMUSP00000156783.2	Nonsense mediated decay		A0A3B2W7Z5	-
ENSMUST00000233957.2	Vmn2r58-207	3826	72aa	ENSMUSP00000156760.2	Nonsense mediated decay		A0A3B2W3G0	-
ENSMUST00000232976.2	Vmn2r58-202	2587	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-

.

Summary

.

.