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

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Gene: Vmn2r67 ENSMUSG00000095664

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Description

vomeronasal 2, receptor 67 [Source:MGI Symbol;Acc:MGI:3643129]

Gene Synonyms

EG620672

Location

Chromosome 7: 84,776,175-84,805,206 reverse strand.

GRCm39:CM001000.3

About this gene

This gene has 5 transcripts (splice variants), 114 orthologues and 128 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000168730.3	Vmn2r67-201	11925	851aa	ENSMUSP00000126007.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS52289	K7N6T2	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,
ENSMUST00000233734.2	Vmn2r67-204	11862	830aa	ENSMUSP00000156643.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding		A0A3B2WCR5	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENSMUST00000233656.2	Vmn2r67-203	11393	255aa	ENSMUSP00000156949.2	Nonsense mediated decay		A0A3B2WDB2	-
ENSMUST00000233789.2	Vmn2r67-205	11330	234aa	ENSMUSP00000156928.2	Nonsense mediated decay		A0A3B2WDB7	-
ENSMUST00000232720.2	Vmn2r67-202	12623	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-

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Summary

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