# USH1 protein network component sans

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21136557](https://www.wikidata.org/wiki/Q21136557)  
**Source**: https://4ort.xyz/entity/ush1-protein-network-component-sans-q21136557


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q495M9)
3. Q20641742
4. [The giant spectrin βV couples the molecular motors to phototransduction and Usher syndrome type I proteins along their trafficking route](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q495M9)
5. [Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q495M9)
6. [LuTHy: a double-readout bioluminescence-based two-hybrid technology for quantitative mapping of protein-protein interactions in mammalian cells](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q495M9)
7. [An organelle-specific protein landscape identifies novel diseases and molecular mechanisms](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q495M9)
8. [The structure of the harmonin/sans complex reveals an unexpected interaction mode of the two Usher syndrome proteins](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q495M9)
9. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q495M9)
10. [Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q495M9)
11. [Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q495M9)
12. Ensembl Release 99