BBS10
Lua error in Module:Infobox_gene at line 33: attempt to index field 'wikibase' (a nil value). Bardet-Biedl syndrome 10, also known as BBS10 is a human gene.[1]
Function
The Bardet-Biedl syndrome 10 protein has distant sequence homology to type II chaperonins. As a molecular chaperone, this protein may affect the folding or stability of other ciliary or basal body proteins. Inhibition of this protein's expression impairs ciliogenesis in preadipocytes.[2]
Clinical significance
Mutations in this gene are associated with the Bardet-Biedl syndrome.[1]
References
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<references />, or <references group="..." />Further reading
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External links
- GeneReviews/NIH/NCBI/UW entry on Bardet-Biedl Syndrome
- Bbs10 protein, human at the US National Library of Medicine Medical Subject Headings (MeSH)
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