# Bardet-Biedl syndrome 12

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21105418](https://www.wikidata.org/wiki/Q21105418)  
**Source**: https://4ort.xyz/entity/bardet-biedl-syndrome-12


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q6ZW61)
3. Q20641742
4. [A novel H395R mutation in MKKS/BBS6 causes retinitis pigmentosa and polydactyly without other findings of Bardet-Biedl or McKusick-Kaufman syndrome](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q6ZW61)
5. [Intrinsic Protein-Protein Interaction-mediated and Chaperonin-assisted Sequential Assembly of Stable Bardet-Biedl Syndrome Protein Complex, the BBSome](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q6ZW61)
6. [BBS6, BBS10, and BBS12 form a complex with CCT/TRiC family chaperonins and mediate BBSome assembly](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q6ZW61)
7. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q6ZW61)
8. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q6ZW61&geneProductId=UniProtKB:Q6ZW61)
9. [BBS-Induced Ciliary Defect Enhances Adipogenesis, Causing Paradoxical Higher-Insulin Sensitivity, Glucose Usage, and Decreased Inflammatory Response](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q6ZW61)
10. Ensembl Release 99