# RPGRIP1 like

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21118164](https://www.wikidata.org/wiki/Q21118164)  
**Source**: https://4ort.xyz/entity/rpgrip1-like


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q68CZ1)
3. Q20641742
4. [Thromboxane A2-induced signal transduction is negatively regulated by KIAA1005 that directly interacts with thromboxane A2 receptor](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q68CZ1)
5. [Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q68CZ1)
6. [A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q68CZ1)
7. [Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q68CZ1)
8. [An organelle-specific protein landscape identifies novel diseases and molecular mechanisms](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q68CZ1)
9. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q68CZ1)
10. [The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q68CZ1)
11. [Novel asymmetrically localizing components of human centrosomes identified by complementary proteomics methods](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q68CZ1)
12. [TMEM107 recruits ciliopathy proteins to subdomains of the ciliary transition zone and causes Joubert syndrome](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q68CZ1&geneProductId=UniProtKB:Q68CZ1)
13. [The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q68CZ1&geneProductId=UniProtKB:Q68CZ1)
14. [TMEM107 recruits ciliopathy proteins to subdomains of the ciliary transition zone and causes Joubert syndrome](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q68CZ1)
15. Ensembl Release 99