# Nephrocystin 3

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21117131](https://www.wikidata.org/wiki/Q21117131)  
**Source**: https://4ort.xyz/entity/nephrocystin-3


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q7Z494)
3. Q20641742
4. [Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q7Z494)
5. [Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q7Z494)
6. [An ARL3-UNC119-RP2 GTPase cycle targets myristoylated NPHP3 to the primary cilium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q7Z494)
7. [Mutations in NEK8 link multiple organ dysplasia with altered Hippo signalling and increased c-MYC expression](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q7Z494)
8. [Structural basis for Arl3-specific release of myristoylated ciliary cargo from UNC119.](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q7Z494)
9. [An organelle-specific protein landscape identifies novel diseases and molecular mechanisms](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q7Z494)
10. [Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q7Z494)
11. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q7Z494)
12. [Nephrocystin-3 is required for ciliary function in zebrafish embryos](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q7Z494)
13. [Identification of a gene for renal-hepatic-pancreatic dysplasia by microarray-based homozygosity mapping](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q7Z494)
14. Ensembl Release 99