Golgi SNAP receptor complex member 2 isoform X13 [Homo sapiens]

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Novel Genetic and Phenotypic Expansion in GOSR2-Related Progressive Myoclonus Epilepsy. [Genes (Basel). 2023]
Novel Genetic and Phenotypic Expansion in GOSR2-Related Progressive Myoclonus Epilepsy.
Hentrich L, Parnes M, Lotze TE, Coorg R, de Koning TJ, Nguyen KM, Yip CK, Jungbluth H, Koy A, Dafsari HS. Genes (Basel). 2023 Sep 25; 14(10). Epub 2023 Sep 25.
A paradoxical genotype-phenotype relationship: Low level of GOSR2 translation from a non-AUG start codon in a family with profound hearing loss. [Hum Mol Genet. 2023]
A paradoxical genotype-phenotype relationship: Low level of GOSR2 translation from a non-AUG start codon in a family with profound hearing loss.
Aburayyan A, Carlson RJ, Rabie GN, Lee MK, Gulsuner S, Walsh T, Avraham KB, Kanaan MN, King MC. Hum Mol Genet. 2023 Jul 4; 32(14):2265-2268.
Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease. [JCI Insight. 2022]
Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease.
Yu M, Tcheandjieu C, Georges A, Xiao K, Tejeda H, Dina C, Le Tourneau T, Fiterau M, Judy R, Tsao NL, et al. JCI Insight. 2022 Feb 8; 7(3). Epub 2022 Feb 8.

RefSeq genomic sequence
See the genomic reference sequence for the GOSR2 gene (NG_031806.3).
RefSeq mRNA
See reference mRNA sequence for the GOSR2 gene (XM_047437119.1).
RefSeq protein isoforms
See 47 reference sequence protein isoforms for the GOSR2 gene.

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Protein