BBS9
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Template:Short description Template:Infobox gene Bardet–Biedl syndrome 9 is a protein that in humans is encoded by the BBS9 gene.[1][2]
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.[3]
Mutations in this gene are associated with the Bardet–Biedl syndrome.[2]
References
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External links
Further reading
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External links
- GeneReviews/NIH/NCBI/UW entry on Bardet–Biedl Syndrome
- Template:Replace at the U.S. National Library of Medicine Medical Subject Headings (MeSH)