# Wolframin ER transmembrane glycoprotein

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21136669](https://www.wikidata.org/wiki/Q21136669)  
**Source**: https://4ort.xyz/entity/wolframin-er-transmembrane-glycoprotein


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/O76024)
3. Q20641742
4. [Sodium-potassium ATPase 1 subunit is a molecular partner of Wolframin, an endoplasmic reticulum protein involved in ER stress](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O76024)
5. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O76024)
6. [Genome-wide YFP fluorescence complementation screen identifies new regulators for telomere signaling in human cells](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O76024)
7. [Wolfram syndrome 1 gene negatively regulates ER stress signaling in rodent and human cells](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O76024)
8. [WFS1 (Wolfram syndrome 1) gene product: predominant subcellular localization to endoplasmic reticulum in cultured cells and neuronal expression in rat brain](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O76024)
9. [Wolframin expression induces novel ion channel activity in endoplasmic reticulum membranes and increases intracellular calcium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O76024)
10. [A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O76024)
11. [Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O76024)
12. [Endoplasmic reticulum stress and Parkinson's disease: the role of HRD1 in averting apoptosis in neurodegenerative disease](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O76024)
13. [Mutations in the WFS1 gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in Japanese](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O76024)
14. [WFS1 protein modulates the free Ca(2+) concentration in the endoplasmic reticulum](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O76024)
15. [Endoplasmic reticulum stress induces Wfs1 gene expression in pancreatic beta-cells via transcriptional activation](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O76024)
16. [Expressional and functional studies of Wolframin, the gene function deficient in Wolfram syndrome, in mice and patient cells](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O76024)
17. ensembl Release 98
18. Transporter Classification database