SLC17A5

Solute carrier family 17 (anion/sugar transporter), member 5, also known as SLC17A5 or sialin, is a protein which in humans is encoded by the SLC17A5 gene.

Clinical significance

A deficiency of this protein causes Salla disease.

The gene for HP59 contains, entirely within its coding region, the Sialin Gene SLC17A5. Member 5, also known as SLC17A5 or sialin is a lysosomal membrane sialic acid transport protein which in humans is encoded by the SLC17A5 gene on Chromosome 6

See also

  • Solute carrier family

    • References

    Further reading

    This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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