# Cholinergic receptor nicotinic delta subunit

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21111180](https://www.wikidata.org/wiki/Q21111180)  
**Source**: https://4ort.xyz/entity/cholinergic-receptor-nicotinic-delta-subunit


## References

1. UniProt
2. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL983)
3. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL1200527)
4. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL1201244)
5. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL1739)
6. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL1201206)
7. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL1200641)
8. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL360055)
9. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL1360)
10. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL1200757)
11. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL1200648)
12. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL1200629)
13. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q07001)
14. Q20641742
15. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q07001)
16. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q07001)
17. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q07001&geneProductId=UniProtKB:Q07001)
18. [New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q07001&geneProductId=UniProtKB:Q07001)
19. [New mutations in acetylcholine receptor subunit genes reveal heterogeneity in the slow-channel congenital myasthenic syndrome](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q07001)
20. [Acetylcholine receptor delta subunit mutations underlie a fast-channel myasthenic syndrome and arthrogryposis multiplex congenita](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q07001)
21. [Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q07001)
22. Ensembl Release 99
23. Transporter Classification database