Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: SLC2A13 ENSPTRG00000004827

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Description

solute carrier family 2 member 13 [Source:VGNC Symbol;Acc:VGNC:8538]

Location

Chromosome 12: 50,037,826-50,370,076 forward strand.

Pan_tro_3.0:CM000326.3

About this gene

This gene has 1 transcript (splice variant), 303 orthologues and 15 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000008935.4	SLC2A13-201	2231	648aa	ENSPTRP00000008252.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2VZA6 H2Q5Q3	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, 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,

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Summary

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