Citations for
1SCAR20, SNX14
Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome.
Thomas AC, Williams H, Setó-Salvia N, Bacchelli C, Jenkins D, O'Sullivan M, Mengrelis K, Ishida M, Ocaka L, Chanudet E, James C, Lescai F, Anderson G, Morrogh D, Ryten M, Duncan AJ, Pai YJ, Saraiva JM, Ramos F, Farren B, Saunders D, Vernay B, Gissen P, Straatmaan-Iwanowska A, Baas F, Wood NW, Hersheson J, Houlden H, Hurst J, Scott R, Bitner-Glindzicz M, Moore GE, Sousa SB, Stanier P.
Am J Hum Genet 95(5):611-21. doi: 10.1016/j.ajhg.2014.10.007. Epub 2014 Nov 6. 2014
2SNX14
Snx14 regulates neuronal excitability, promotes synaptic transmission, and is imprinted in the brain of mice.
Huang HS, Yoon BJ, Brooks S, Bakal R, Berrios J, Larsen RS, Wallace ML, Han JE, Chung EH, Zylka MJ, Philpot BD.
PLoS One 9(5):e98383. doi: 10.1371/journal.pone.0098383. eCollection 2014. 2014
3ARHGAP33, SNX1, SNX10, SNX11, SNX12, SNX13, SNX14, SNX16, SNX18, SNX2, SNX21, SNX27, SNX4, SNX5, SNX6, SNX7, SNX8, SNX9
A large family of endosome-localized proteins related to sorting nexin 1.
Teasdale RD, Loci D, Houghton F, Karlsson L, Gleeson PA.
Biochem J 358(Pt 1):7-16. 2001
4SNX14
Sorting nexin-14, a gene expressed in motoneurons trapped by an in vitro preselection method.
Carroll P, Renoncourt Y, Gayet O, De Bovis B, Alonso S.
Dev Dyn 221(4):431-42. 2001