Gene: Vmn1r66 ENSMUSG00000043066

Description

vomeronasal 1 receptor 66 [Source:MGI Symbol;Acc:MGI:2159633]

Gene Synonyms

V1re11

Location

Chromosome 7: 10,006,918-10,011,933 reverse strand.

GRCm39:CM001000.3

About this gene

This gene has 5 transcripts (splice variants), 107 orthologues and 237 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000228622.2	Vmn1r66-205	3304	310aa	ENSMUSP00000153860.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS20790	Q8K4I0	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, GENCODE Primary represents a minimal set that contains MANE Select, MANE Plus Clinical and Ensembl Canonical transcripts and transcripts containing any conserved exons and common alternative splicing events (including exons skips) that are absent from the MANE and Ensembl Canonical transcripts for protein-coding genes. Other biotypes will have the GENCODE Primary flag added to the Ensembl Canonical transcript and for lncRNA genes only this will be the transcripts with the longest genomic span.GENCODE Primary, A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.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,
ENSMUST00000228086.2	Vmn1r66-204	3013	310aa	ENSMUSP00000153825.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS20790	Q8K4I0	A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.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,
ENSMUST00000227719.2	Vmn1r66-203	2765	310aa	ENSMUSP00000154063.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS20790	Q8K4I0	A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.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,
ENSMUST00000060374.5	Vmn1r66-201	1524	310aa	ENSMUSP00000055861.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS20790	Q8K4I0	A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.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 NA: A transcript that was not analysed for TSL. 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:NA,
ENSMUST00000226202.2	Vmn1r66-202	3345	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-

Strains

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

Gene: Vmn1r66 ENSMUSG00000043066

Strains

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Gene: Vmn1r66 ENSMUSG00000043066

Strains

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