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: Or10al7 ENSMUSG00000081724

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Description

olfactory receptor family 10 subfamily AL member 7 [Source:MGI Symbol;Acc:MGI:2177512]

Gene Synonyms

GA_x6K02T2PSCP-2503741-2502776, MOR263-9, Olfr129

Location

Chromosome 17: 38,361,748-38,370,970 reverse strand.

GRCm39:CM001010.3

About this gene

This gene has 2 transcripts (splice variants), 117 orthologues and 217 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000122318.4	Or10al7-201	993	330aa	ENSMUSP00000113564.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding		Q8VEY1	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 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,
ENSMUST00000216476.2	Or10al7-202	5275	321aa	ENSMUSP00000149327.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS28772	Q7TRI9	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 3: A transcript where the only support is from a single EST 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:3,

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Summary

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