# Intraflagellar transport 140

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21119795](https://www.wikidata.org/wiki/Q21119795)  
**Source**: https://4ort.xyz/entity/intraflagellar-transport-140


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q96RY7)
3. Q20641742
4. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q96RY7)
5. [Ciliopathy-associated mutations of IFT122 impair ciliary protein trafficking but not ciliogenesis](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q96RY7)
6. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q96RY7&geneProductId=UniProtKB:Q96RY7)
7. [Mainzer-Saldino syndrome is a ciliopathy caused by IFT140 mutations](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q96RY7&geneProductId=UniProtKB:Q96RY7)
8. [Combined NGS approaches identify mutations in the intraflagellar transport gene IFT140 in skeletal ciliopathies with early progressive kidney Disease](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q96RY7)
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?protein=Q96RY7&geneProductId=UniProtKB:Q96RY7)
10. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q96RY7)
11. [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:Q96RY7)
12. [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:Q96RY7)
13. [Mainzer-Saldino syndrome is a ciliopathy caused by IFT140 mutations](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q96RY7)
14. [Partial uniparental isodisomy of chromosome 16 unmasks a deleterious biallelic mutation in IFT140 that causes Mainzer-Saldino syndrome](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q96RY7)
15. Ensembl Release 99