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: Or1e19 ENSMUSG00000055971

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Description

olfactory receptor family 1 subfamily E member 19 [Source:MGI Symbol;Acc:MGI:3030212]

Gene Synonyms

GA_x6K02T2P1NL-3586282-3585338, MOR135-2, Olfr378

Location

Chromosome 11: 73,315,435-73,319,303 reverse strand.

GRCm39:CM001004.3

About this gene

This gene has 1 transcript (splice variant), 135 orthologues and 339 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000069790.5	Or1e19-201	1508	314aa	ENSMUSP00000066971.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS25009	Q8VGT2	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 2: A transcript where the best supporting mRNA is flagged as suspect or the support is from multiple ESTs 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:2,

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Summary

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