golgin subfamily A member 2 isoform 10 [Homo sapiens]

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Bi-allelic loss of function variants in GOLGA2 are associated with a complex neurological phenotype: Report of a second family. [Clin Genet. 2021]
Bi-allelic loss of function variants in GOLGA2 are associated with a complex neurological phenotype: Report of a second family.
Kotecha U, Mistri M, Shah N, Shah PS, Gupta VA. Clin Genet. 2021 Dec; 100(6):748-751. Epub 2021 Aug 29.
Liquid-liquid phase separation of the Golgi matrix protein GM130. [FEBS Lett. 2020]
Liquid-liquid phase separation of the Golgi matrix protein GM130.
Rebane AA, Ziltener P, LaMonica LC, Bauer AH, Zheng H, López-Montero I, Pincet F, Rothman JE, Ernst AM. FEBS Lett. 2020 Apr; 594(7):1132-1144. Epub 2019 Dec 26.
Identification of the interaction of VP1 with GM130 which may implicate in the pathogenesis of CVB3-induced acute pancreatitis. [Sci Rep. 2015]
Identification of the interaction of VP1 with GM130 which may implicate in the pathogenesis of CVB3-induced acute pancreatitis.
Li X, Xia Y, Huang S, Liu F, Ying Y, Xu Q, Liu X, Jin G, Papasian CJ, Chen J, et al. Sci Rep. 2015 Aug 28; 5:13324. Epub 2015 Aug 28.

RefSeq mRNA
See reference mRNA sequence for the GOLGA2 gene (NM_001389702.2).
RefSeq protein isoforms
See 14 reference sequence protein isoforms for the GOLGA2 gene.

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