# Usherin

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21136556](https://www.wikidata.org/wiki/Q21136556)  
**Source**: https://4ort.xyz/entity/usherin


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/O75445)
3. Q20641742
4. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O75445)
5. [A domain-specific usherin/collagen IV interaction may be required for stable integration into the basement membrane superstructure](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O75445)
6. [The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O75445)
7. [PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O75445)
8. [Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O75445)
9. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O75445)
10. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=O75445&geneProductId=UniProtKB:O75445)
11. [Usherin expression is highly conserved in mouse and human tissues](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O75445)
12. [A mutation (2314delG) in the Usher syndrome type IIA gene: high prevalence and phenotypic variation](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O75445)
13. [Disease expression in Usher syndrome caused by VLGR1 gene mutation (USH2C) and comparison with USH2A phenotype](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O75445)
14. Ensembl Release 99