# Bardet-Biedl syndrome 2 (human)

> mammalian protein found in Mus musculus

**Wikidata**: [Q21418946](https://www.wikidata.org/wiki/Q21418946)  
**Source**: https://4ort.xyz/entity/bardet-biedl-syndrome-2-human-


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q9CWF6)
3. Entrez Gene
4. [DAZ-interacting Protein 1 (Dzip1) Phosphorylation by Polo-like Kinase 1 (Plk1) Regulates the Centriolar Satellite Localization of the BBSome Protein during the Cell Cycle](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9CWF6)
5. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9CWF6)
6. [The BBSome controls IFT assembly and turnaround in cilia](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9CWF6)
7. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9CWF6)
8. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9CWF6&geneProductId=UniProtKB:Q9CWF6)
9. [The Centriolar Satellite Protein AZI1 Interacts with BBS4 and Regulates Ciliary Trafficking of the BBSome](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9CWF6&geneProductId=UniProtKB:Q9CWF6)
10. [BBS6, BBS10, and BBS12 form a complex with CCT/TRiC family chaperonins and mediate BBSome assembly](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9CWF6&geneProductId=UniProtKB:Q9CWF6)
11. [A Novel Protein LZTFL1 Regulates Ciliary Trafficking of the BBSome and Smoothened](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9CWF6&geneProductId=UniProtKB:Q9CWF6)
12. [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?protein=Q9CWF6&geneProductId=UniProtKB:Q9CWF6)
13. [Bardet-Biedl syndrome 3 (Bbs3) knockout mouse model reveals common BBS-associated phenotypes and Bbs3 unique phenotypes](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9CWF6&geneProductId=UniProtKB:Q9CWF6)
14. [Ciliary proteins Bbs8 and Ift20 promote planar cell polarity in the cochlea](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9CWF6)
15. [Loss of Bardet–Biedl syndrome proteins alters the morphology and function of motile cilia in airway epithelia](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9CWF6&geneProductId=UniProtKB:Q9CWF6)
16. [Bardet-Biedl syndrome 3 (Bbs3) knockout mouse model reveals common BBS-associated phenotypes and Bbs3 unique phenotypes](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9CWF6)
17. [Loss of Bardet–Biedl syndrome proteins alters the morphology and function of motile cilia in airway epithelia](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9CWF6)
18. [The Centriolar Satellite Protein AZI1 Interacts with BBS4 and Regulates Ciliary Trafficking of the BBSome](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9CWF6)
19. [A Novel Protein LZTFL1 Regulates Ciliary Trafficking of the BBSome and Smoothened](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9CWF6)
20. [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:Q9CWF6)
21. [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:Q9CWF6)
22. [Bardet–Biedl syndrome proteins are required for the localization of G protein-coupled receptors to primary cilia](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9CWF6)
23. [Bbs2 -null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9CWF6)
24. [BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypes](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9CWF6)
25. [Requirement of Bardet-Biedl syndrome proteins for leptin receptor signaling](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9CWF6)
26. [Contrasting vascular effects caused by loss of Bardet-Biedl syndrome genes](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9CWF6)
27. [Leptin resistance contributes to obesity and hypertension in mouse models of Bardet-Biedl syndrome](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9CWF6)
28. [Cartilage abnormalities associated with defects of chondrocytic primary cilia in Bardet‐Biedl syndrome mutant mice](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9CWF6)
29. [A knockin mouse model of the Bardet–Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesity](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9CWF6)
30. [Temporal expression pattern of Bardet-Biedl syndrome genes in adipogenesis](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9CWF6)
31. ensembl Release 106