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GeneQ7390842· pop 8· linked from 264 articles

Also known as solute carrier family 2 (facilitated glucose transporter), member 9, GLUT9, GLUTX, UAQTL2, URATv1, solute carrier family 2 member 9

Solute carrier family 2, facilitated glucose transporter member 9 is a protein that in humans is encoded by the SLC2A9 gene.

In the Vinony graph

Vinony's link graph records 264 inbound references to SLC2A9, and connects out to PubMed, Ensembl genome database project and transmembrane transport proteins.

Vinony files it under Genes on human chromosome 4 and Solute carrier family.

Vinony links it to 7 Wikipedia language editions.

Gene data

SLC2A9
Name
solute carrier family 2 member 9
Type
protein-coding
Position
9,771,148–10,054,936 (−)
Aliases
GLUT9, GLUTX, UAQTL2, URATv1
RefSeq RNA
NM_001001290.2, NM_020041.3, XM_006713968.5, XM_011513856.4, XM_011513858.2
RefSeq protein
NP_001001290.1, NP_064425.2, XP_006714031.1, XP_011512158.1, XP_011512160.1

This gene encodes a member of the SLC2A facilitative glucose transporter family. Members of this family play a significant role in maintaining glucose homeostasis. The encoded protein may play a role in the development and survival of chondrocytes in cartilage matrices. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008].

via MyGene.info

Gene · Ensembl

solute carrier family 2 member 9

Symbol
SLC2A9
Biotype
Protein coding
Organism
Homo sapiens
Location
4:9,771,148-10,054,936
Strand
Reverse (−)
Assembly
GRCh38
View on Ensembl →

via Ensembl · EMBL-EBI

Wikidata facts

Instance of
gene
Show 10 more facts
HomoloGene ID
69290
genetic association
gout
found in taxon
Homo sapiens
genomic end
10056560
genomic start
9772777
cytogenetic location
4p16.1
expressed in
salivary gland
Commons category
Glucose transporter 9
Sources (5)

via Wikidata · CC0

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Encyclopedic overview

3 sections
Contents
  • See also
  • References
  • Further reading

Solute carrier family 2, facilitated glucose transporter member 9 is a protein that in humans is encoded by the SLC2A9 gene.

This gene encodes a member of the SLC2A facilitative glucose transporter family. Members of this family play a significant role in maintaining glucose homeostasis. The encoded protein may play a role in the development and survival of chondrocytes in cartilage matrices. Two transcript variants encoding distinct isoforms have been identified for this gene.

Excerpted from Wikipedia’s “SLC2A9” article, available under the CC BY-SA 4.0 licence.

Available in 7 languages

via Wikidata sitelinks · CC0

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