- Gene Overview
- Interaction Network
- Sequence Verification
SLC17A5, solute carrier family 17 member 5
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This gene encodes a membrane transporter that exports free sialic acids that have been cleaved off of cell surface lipids and proteins from lysosomes. Mutations in this gene cause sialic acid storage diseases, including infantile sialic acid storage disorder and and Salla disease, an adult form. [provided by RefSeq, Jul 2008]
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Gene Synonyms (sialin, H(+)/nitrate cotransporter, H(+)/sialic acid cotransporter, membrane glycoprotein HP59, sialic acid storage disease, sodium/sialic acid cotransporter, solute carrier family 17 (acidic sugar transporter), member 5, solute carrier family 17 (anion/sugar transporter), member 5, vesicular H(+)/Aspartate-glutamate cotransporter, AST, ISSD, NSD, SD, SIALIN, SIASD, SLD,)
- NCBI Gene ID:
26503
- Species:
Homo sapiens (Human)
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UNIPROT ID#>>Q9NRA2
- 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 17 member 5 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.
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