# Whirlin

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21174295](https://www.wikidata.org/wiki/Q21174295)  
**Source**: https://4ort.xyz/entity/whirlin-q21174295


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q9P202)
3. Q20641742
4. [Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48.](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P202)
5. [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:Q9P202)
6. [MPP1 links the Usher protein network and the Crumbs protein complex in the retina](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P202)
7. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P202)
8. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9P202&geneProductId=UniProtKB:Q9P202)
9. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9P202&geneProductId=UniProtKB:Q9P202)
10. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P202)
11. [A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9P202&geneProductId=UniProtKB:Q9P202)
12. [A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P202)
13. Ensembl Release 99