Gene: Or14c44 ENSMUSG00000061549

Description

olfactory receptor family 14 subfamily C member 44 [Source:MGI Symbol;Acc:MGI:3030135]

Gene Synonyms

GA_x6K02T2NHDJ-9693313-9692378, GA_x6K02T2NHDJ-9695951-9695766, MOR211-8P, MOR221-1P, MOR221-4, Olfr1531-ps1, Olfr301, Olfr302

Location

Chromosome 7: 86,053,054-86,063,232 forward strand.

GRCm39:CM001000.3

About this gene

This gene has 1 transcript (splice variant), 120 orthologues and 392 paralogues.

Transcripts

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Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000174362.3	Or14c44-201	1937	311aa	ENSMUSP00000133780.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS57560	Q7TS04	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, 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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Gene: Or14c44 ENSMUSG00000061549

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Gene: Or14c44 ENSMUSG00000061549

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