| 1 | RNF170, SNAX1 |
| A mutation in the RNF170 gene causes autosomal dominant sensory ataxia. | |
| Valdmanis PN, Dupré N, Lachance M, Stochmanski SJ, Belzil VV, Dion PA, Thiffault I, Brais B, Weston L, Saint-Amant L, Samuels ME, Rouleau GA. | |
| Brain 134(Pt 2):602-7. Epub 2010 Nov 28. 2011 | |
| 2 | ITPR1, RNF170 |
| RNF170 protein, an endoplasmic reticulum membrane ubiquitin ligase, mediates inositol 1,4,5-trisphosphate receptor ubiquitination and degradation. | |
| Lu JP, Wang Y, Sliter DA, Pearce MM, Wojcikiewicz RJ. | |
| J Biol Chem 286(27):24426-33. Epub 2011 May 24. 2011 | |