# NACC1

> protein-coding gene in the species Homo sapiens

**Wikidata**: [Q18048880](https://www.wikidata.org/wiki/Q18048880)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/BTBD14B)  
**Source**: https://4ort.xyz/entity/nacc1


## References

1. ensembl Release 106
2. Ensembl Release 87
3. Q20641742
4. Online Mendelian Inheritance in Man
5. HomoloGene build68
6. [Orthologous MAtrix](https://omabrowser.org/oma/vps/Q96RE7/)
7. UniProt
8. [Phenocarta](https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_9970&ncbiId=112939)
9. A Recurrent De Novo Variant in NACC1 Causes a Syndrome Characterized by Infantile Epilepsy, Cataracts, and Profound Developmental Delay
10. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000160877/MONDO_0044306)
11. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000069)
12. UMLS 2023
13. [Bgee](https://www.bgee.org/gene/ENSG00000160877)