# Solute carrier family 30 member 9

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21136810](https://www.wikidata.org/wiki/Q21136810)  
**Source**: https://4ort.xyz/entity/solute-carrier-family-30-member-9


## References

1. UniProt
2. [BioGRID](https://thebiogrid.org/news/227)
3. Q20641742
4. [The novel human HUEL (C4orf1) gene maps to chromosome 4p12-p13 and encodes a nuclear protein containing the nuclear receptor interaction motif](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q6PML9)
5. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q6PML9)
6. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q6PML9&geneProductId=UniProtKB:Q6PML9)
7. [A census of human transcription factors: function, expression and evolution](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q6PML9)
8. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q6PML9)
9. [The novel human HUEL (C4orf1) gene maps to chromosome 4p12-p13 and encodes a nuclear protein containing the nuclear receptor interaction motif](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q6PML9&geneProductId=UniProtKB:Q6PML9)
10. [SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndrome](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q6PML9&geneProductId=UniProtKB:Q6PML9)
11. [SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndrome](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q6PML9)
12. [Zinc transporter 2 (SLC30A2) can suppress the vesicular zinc defect of adaptor protein 3-depleted fibroblasts by promoting zinc accumulation in lysosomes](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q6PML9)
13. Ensembl Release 99
14. Transporter Classification database