BBS10

Bardet–Biedl syndrome 10, also known as BBS10 is a human gene.

BBS10
Identifiers
Aliases	BBS10, C12orf58, Bardet-Biedl syndrome 10
External IDs	OMIM: 610148; MGI: 1919019; HomoloGene: 49781; GeneCards: BBS10; OMA:BBS10 - orthologs
Gene location (Human) Chr. Chromosome 12 (human) Band 12q21.2 Start 76,344,474 bp End 76,348,415 bp
Gene location (Mouse) Chr. Chromosome 10 (mouse) Band 10|10 D1 Start 111,134,540 bp End 111,137,588 bp
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 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
Wikidata
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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.

Clinical significance

Mutations in this gene are associated with the Bardet–Biedl syndrome.

Further reading

• Stoetzel C, Muller J, Laurier V, et al. (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". Am. J. Hum. Genet. 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 Res. 48 (3): 392–9. doi:10.1016/j.visres.2007.08.024. PMC 2584151. PMID 17980398.
• White DR, Ganesh A, Nishimura D, et al. (2007). "Autozygosity mapping of Bardet-Biedl syndrome to 12q21.2 and confirmation of FLJ23560 as BBS10". Eur. J. Hum. Genet. 15 (2): 173–8. doi:10.1038/sj.ejhg.5201736. PMID 17106446.
• Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
• Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
• Dollfus H, Muller J, Stoetzel C, et al. (2006). "[Bardet-Biedl syndrome: a unique family for a major gene (BBS10)]" (PDF). Med Sci (Paris). 22 (11): 901–4. doi:10.1051/medsci/20062211901. PMID 17101080.
• Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
• Marion V, Stoetzel C, Schlicht D, et al. (2009). "Transient ciliogenesis involving Bardet-Biedl syndrome proteins is a fundamental characteristic of adipogenic differentiation". Proc. Natl. Acad. Sci. U.S.A. 106 (6): 1820–5. Bibcode:2009PNAS..106.1820M. doi:10.1073/pnas.0812518106. PMC 2635307. PMID 19190184.
• Laurier V, Stoetzel C, Muller J, et al. (2006). "Pitfalls of homozygosity mapping: an extended consanguineous Bardet-Biedl syndrome family with two mutant genes (BBS2, BBS10), three mutations, but no triallelism". Eur. J. Hum. Genet. 14 (11): 1195–203. doi:10.1038/sj.ejhg.5201688. PMID 16823392.
• Strausberg RL, Feingold EA, Grouse LH, et al. (2002). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
• Kimura K, Wakamatsu A, Suzuki Y, et al. (2006). "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes". Genome Res. 16 (1): 55–65. doi:10.1101/gr.4039406. PMC 1356129. PMID 16344560.
• Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. 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.