SLC2A10

Also known as ATS, GLUT10, solute carrier family 2 member 10, ATORS

Solute carrier family 2, facilitated glucose transporter member 10 is a protein that in humans is encoded by the SLC2A10 gene.

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Vinony's link graph records 297 inbound references to SLC2A10, and connects out to PubMed, Ensembl genome database project and transmembrane transport proteins.

It sits within the topics Genes on human chromosome 20 and Solute carrier family.

Vinony links it to 4 Wikipedia language editions.

Gene data

SLC2A10

Name: solute carrier family 2 member 10
Type: protein-coding
Position: 46,709,577–46,737,312 (+)
Aliases: ATORS, ATS, GLUT10
Ensembl: ENSG00000197496
RefSeq RNA: NM_030777.4, XM_011529060.3, XM_011529061.3, XM_011529062.3, XM_011529063.3
RefSeq protein: NP_110404.1, XP_011527362.1, XP_011527363.1, XP_011527364.1, XP_011527365.1

This gene encodes a member of the class III facilitative glucose transporter family. The encoded protein plays a role in regulation of glucose homeostasis. Mutations in this gene have been associated with arterial tortuosity syndrome.[provided by RefSeq, Dec 2009].

Pathways

Disease Cellular hexose transport Transport of small molecules SLC-mediated transmembrane transport Defective SLC2A10 causes arterial tortuosity syndrome (ATS)SLC transporter disorders Disorders of transmembrane transporters Nuclear Receptors Meta-Pathway NRF2 pathway

via MyGene.info

Gene · Ensembl

solute carrier family 2 member 10

Symbol: SLC2A10
Biotype: Protein coding
Organism: Homo sapiens
Location: 20:46,709,577-46,737,312
Strand: Forward (+)
Assembly: GRCh38

View on Ensembl →

via Ensembl · EMBL-EBI

Wikidata facts

Instance of: gene

Show 9 more facts

HomoloGene ID: 38551
found in taxon: Homo sapiens
exact match: identifiers.org/ncbigene/81031
chromosome: human chromosome 20
genomic start: 46709649
genomic end: 45364965
cytogenetic location: 20q13.12
genetic association: arterial tortuosity syndrome
Commons category: Glucose transporter 10

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Encyclopedic overview

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Contents

See also
References
Further reading

Solute carrier family 2, facilitated glucose transporter member 10 is a protein that in humans is encoded by the SLC2A10 gene.

SLC2A10 is a member of the facilitative glucose transporter family, which plays a significant role in maintaining glucose homeostasis.[supplied by OMIM]

Excerpted from Wikipedia’s “SLC2A10” article, available under the CC BY-SA 4.0 licence.