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

Configure this page

Share this page

Bookmark this page

.

Gene: SLC2A8 ENSPTRG00000021387

.

Description

solute carrier family 2 member 8 [Source:VGNC Symbol;Acc:VGNC:8933]

Location

Chromosome 9: 105,508,364-105,519,165 forward strand.

Pan_tro_3.0:CM000323.3

About this gene

This gene has 2 transcripts (splice variants), 260 orthologues and 15 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000039565.5	SLC2A8-201	2171	477aa	ENSPTRP00000036554.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2VZ83 H2QXX2	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,
ENSPTRT00000079802.1	SLC2A8-202	2019	411aa	ENSPTRP00000071558.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3S3P4 A0A6D2VTK2	-

.

Summary

.

.