Gene: Slc2a13 ENSMUSG00000036298

Description

solute carrier family 2 (facilitated glucose transporter), member 13 [Source:MGI Symbol;Acc:MGI:2146030]

Gene Synonyms

A630029G22Rik

Location

Chromosome 15: 91,151,898-91,457,464 reverse strand.

GRCm39:CM001008.3

About this gene

This gene has 7 transcripts (splice variants), 308 orthologues, 11 paralogues and is associated with 5 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	Flags
ENSMUST00000109283.3	Slc2a13-202	6537	637aa	ENSMUSP00000104906.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS27761	Q3UHK1	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 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. 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:1,
ENSMUST00000402925.1	Slc2a13-206	2843	429aa	ENSMUSP00000181288.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		-	A subset of the GENCODE transcript set, containing only 5' and 3' complete transcripts at protein-coding genes.GENCODE Basic,
ENSMUST00000402923.1	Slc2a13-204	6837	187aa	ENSMUSP00000181286.1	Nonsense mediated decay		-	-
ENSMUST00000402924.1	Slc2a13-205	6348	331aa	ENSMUSP00000181287.1	Nonsense mediated decay		-	-
ENSMUST00000402926.1	Slc2a13-207	2706	331aa	ENSMUSP00000181289.1	Nonsense mediated decay		-	-
ENSMUST00000109282.2	Slc2a13-201	2081	No protein	-	Alternatively spliced transcript of a protein coding gene for which we cannot define a CDS.Protein coding CDS not defined		-	TSL 1: A transcript where all splice junctions are supported by at least one non-suspect mRNA. 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:1,
ENSMUST00000156971.2	Slc2a13-203	479	No protein	-	Alternatively spliced transcript of a protein coding gene for which we cannot define a CDS.Protein coding CDS not defined		-	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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Gene: Slc2a13 ENSMUSG00000036298

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Gene: Slc2a13 ENSMUSG00000036298

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