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: Or8b40 ENSMUSG00000096356

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Description

olfactory receptor family 8 subfamily B member 40 [Source:MGI Symbol;Acc:MGI:3030723]

Gene Synonyms

GA_x6K02T2PVTD-31795028-31795957, MOR162-2, Olfr889

Location

Chromosome 9: 38,026,494-38,032,541 forward strand.

GRCm39:CM001002.3

About this gene

This gene has 2 transcripts (splice variants), 57 orthologues and 393 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000072290.5	Or8b40-201	945	314aa	ENSMUSP00000072137.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding		L7N1Y6	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, 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,
ENSMUST00000217286.2	Or8b40-202	5673	309aa	ENSMUSP00000148913.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS85655	Q9EQA4	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,

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Summary

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