# Protocadherin related 15

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21121853](https://www.wikidata.org/wiki/Q21121853)  
**Source**: https://4ort.xyz/entity/protocadherin-related-15


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q96QU1)
3. Q20641742
4. [Swiss-Prot](http://www.uniprot.org/uniprot/Q99PJ1.txt?version=124)
5. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q96QU1)
6. [PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q96QU1)
7. [Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q96QU1)
8. [Protocadherin 15 (PCDH15): a new secreted isoform and a potential marker for NK/T cell lymphomas](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q96QU1&geneProductId=UniProtKB:Q96QU1)
9. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q96QU1)
10. [Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q96QU1)
11. [Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q96QU1)
12. [Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q96QU1)
13. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q96QU1&geneProductId=UniProtKB:Q96QU1)
14. Ensembl Release 99