# WD repeat domain 35

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21122969](https://www.wikidata.org/wiki/Q21122969)  
**Source**: https://4ort.xyz/entity/wd-repeat-domain-35


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q9P2L0)
3. Q20641742
4. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2L0)
5. [Ciliopathy-associated mutations of IFT122 impair ciliary protein trafficking but not ciliogenesis](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2L0)
6. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2L0)
7. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9P2L0&geneProductId=UniProtKB:Q9P2L0)
8. [TULP3 bridges the IFT-A complex and membrane phosphoinositides to promote trafficking of G protein-coupled receptors into primary cilia](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9P2L0&geneProductId=UniProtKB:Q9P2L0)
9. [TULP3 bridges the IFT-A complex and membrane phosphoinositides to promote trafficking of G protein-coupled receptors into primary cilia](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2L0)
10. [Intraflagellar transport-A complex mediates ciliary entry and retrograde trafficking of ciliary G protein-coupled receptors.](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2L0)
11. [Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9P2L0)
12. Ensembl Release 99
13. [Identifiers.org](https://registry.identifiers.org/registry/uniprot)