BBS10

BBS10
Identifiers
Aliases	BBS10, C12orf58, Bardet-Biedl syndrome 10
External IDs	OMIM: 610148; MGI: 1919019; GeneCards: BBS10
Gene location (Human) Chr. Chromosome 12 (human)[1] Band 12q21.2 Start 76,344,474 bp[1] End 76,348,415 bp[1]
Gene location (Mouse) Chr. Chromosome 10 (mouse)[2] Band 10|10 D1 Start 111,134,540 bp[2] End 111,137,588 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in Achilles tendon endothelial cell ventricular zone ganglionic eminence Epithelium of choroid plexus retinal pigment epithelium Brodmann area 23 germinal epithelium islet of Langerhans bronchial epithelial cell Top expressed in spermatocyte otolith organ spermatid utricle genital tubercle lumbar spinal ganglion seminiferous tubule zygote tail of embryo oocyte More reference expression data BioGPS n/a
Gene ontology Molecular function nucleotide binding protein binding ATP binding Cellular component cell projection cilium Biological process photoreceptor cell maintenance retina homeostasis regulation of protein-containing complex assembly chaperone-mediated protein complex assembly response to stimulus visual perception non-motile cilium assembly Sources:Amigo / QuickGO
Orthologs Databases NCBI: entry; OMA: entry Species Human Mouse Entrez 79738 71769 Ensembl ENSG00000179941 ENSMUSG00000035759 UniProt Q8TAM1 Q9DBI2 RefSeq (mRNA) NM_024685 NM_027914 RefSeq (protein) NP_078961 NP_082190 Location (UCSC) Chr 12: 76.34 – 76.35 Mb Chr 10: 111.13 – 111.14 Mb PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

BBSome complex assembly protein BBS10, also known as Bardet–Biedl syndrome 10 protein, is encoded in the human by the BBS10 gene.^[5][6]

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.^[7][8]

Clinical significance

Mutations in this gene are associated with the Bardet–Biedl syndrome.^[6]

References

1. GRCh38: Ensembl release 89: ENSG00000179941 – Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000035759 – Ensembl, May 2017
3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
5. "UniProt". UniProt. Retrieved 17 June 2026.
6. Stoetzel C, Laurier V, Davis EE, Muller J, Rix S, Badano JL, et al. (May 2006). "BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus". Nature Genetics. 38 (5): 521–524. doi:10.1038/ng1771. PMID 16582908. S2CID 32269156.
7. "Entrez Gene: Bardet-Biedl syndrome 10".
8. Maruyama K, Sugano S (January 1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–174. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.

Further reading

• Stoetzel C, Muller J, Laurier V, Davis EE, Zaghloul NA, Vicaire S, et al. (January 2007). "Identification of a novel BBS gene (BBS12) highlights the major role of a vertebrate-specific branch of chaperonin-related proteins in Bardet-Biedl syndrome". American Journal of Human Genetics. 80 (1): 1–11. doi:10.1086/510256. PMC 1785304. PMID 17160889.
• Gerth C, Zawadzki RJ, Werner JS, Héon E (2008). "Retinal morphology in patients with BBS1 and BBS10 related Bardet-Biedl Syndrome evaluated by Fourier-domain optical coherence tomography". Vision Research. 48 (3): 392–399. doi:10.1016/j.visres.2007.08.024. PMC 2584151. PMID 17980398.
• White DR, Ganesh A, Nishimura D, Rattenberry E, Ahmed S, Smith UM, et al. (February 2007). "Autozygosity mapping of Bardet-Biedl syndrome to 12q21.2 and confirmation of FLJ23560 as BBS10". European Journal of Human Genetics. 15 (2): 173–178. doi:10.1038/sj.ejhg.5201736. PMID 17106446.
• Dollfus H, Muller J, Stoetzel C, Laurier V, Bonneau D, Mégarbané A, et al. (November 2006). "[Bardet-Biedl syndrome: a unique family for a major gene (BBS10)]". Medecine Sciences. 22 (11): 901–904. doi:10.1051/medsci/20062211901. PMID 17101080.

• Marion V, Stoetzel C, Schlicht D, Messaddeq N, Koch M, Flori E, et al. (February 2009). "Transient ciliogenesis involving Bardet-Biedl syndrome proteins is a fundamental characteristic of adipogenic differentiation". Proceedings of the National Academy of Sciences of the United States of America. 106 (6): 1820–1825. Bibcode:2009PNAS..106.1820M. doi:10.1073/pnas.0812518106. PMC 2635307. PMID 19190184.
• Laurier V, Stoetzel C, Muller J, Thibault C, Corbani S, Jalkh N, et al. (November 2006). "Pitfalls of homozygosity mapping: an extended consanguineous Bardet-Biedl syndrome family with two mutant genes (BBS2, BBS10), three mutations, but no triallelism". European Journal of Human Genetics. 14 (11): 1195–1203. doi:10.1038/sj.ejhg.5201688. PMID 16823392.
• Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, Suyama A, Sugano S (October 1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–156. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.

External links

• GeneReviews/NIH/NCBI/UW entry on Bardet-Biedl Syndrome
• Bbs10 protein, human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
• Human BBS10 genome location and BBS10 gene details page in the UCSC Genome Browser.