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: Vmn2r94 ENSMUSG00000090417

.

Description

vomeronasal 2, receptor 94 [Source:MGI Symbol;Acc:MGI:3648050]

Gene Synonyms

EG665227

Location

Chromosome 17: 18,461,384-18,498,018 reverse strand.

GRCm39:CM001010.3

About this gene

This gene has 4 transcripts (splice variants), 131 orthologues and 128 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000172190.4	Vmn2r94-201	5153	818aa	ENSMUSP00000126386.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS49971	E9PZK8	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,
ENSMUST00000231815.3	Vmn2r94-204	9423	469aa	ENSMUSP00000156288.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A338P793	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENSMUST00000231457.2	Vmn2r94-203	5538	41aa	ENSMUSP00000155968.2	Nonsense mediated decay		A0A338P6T7	-
ENSMUST00000231390.2	Vmn2r94-202	3783	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-

.

Summary

.

.