SLC2A9, solute carrier family 2 member 9

SLC2A9, solute carrier family 2 member 9

• 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]

• Gene Synonyms (GLUT9, GLUTX, UAQTL2, URATv1, solute carrier family 2, facilitated glucose transporter member 9, GLUT-9, glucose transporter type 9, human glucose transporter-like protein-9, solute carrier family 2 (facilitated glucose transporter), member 9, urate transporter, urate voltage-driven efflux transporter 1,)
• NCBI Gene ID: 56606
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q9NRM0
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

solute carrier family 2 member 9 interacts with:

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.