BBS9
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Bardet–Biedl syndrome 9 is a protein that in humans is encoded by the BBS9 gene.
The expression of the Bardet–Biedl syndrome 9 protein is downregulated by parathyroid hormone in osteoblastic cells, and therefore, is thought to be involved in parathyroid hormone action in bones.
Mutations in this gene are associated with the Bardet–Biedl syndrome.
External links
- Humangenome location andgene details page in theUCSC Genome Browser.
Further reading
External links
- at the U.S. National Library of MedicineMedical Subject Headings(MeSH)