Homo sapiens glucosylceramidase beta 1 (GBA1), transcript variant 4, m - Nucleotide

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Altered TFEB subcellular localization in nigral neurons of subjects with incidental, sporadic and GBA-related Lewy body diseases. [Acta Neuropathol. 2024]
Altered TFEB subcellular localization in nigral neurons of subjects with incidental, sporadic and GBA-related Lewy body diseases.
Moors TE, Morella ML, Bertran-Cobo C, Geut H, Udayar V, Timmermans-Huisman E, Ingrassia AMT, Brevé JJP, Bol JGJM, Bonifati V, et al. Acta Neuropathol. 2024 Apr 6; 147(1):67. Epub 2024 Apr 6.
GBA1 as a risk gene for osteoporosis in the specific populations and its role in the development of Gaucher disease. [Orphanet J Rare Dis. 2024]
GBA1 as a risk gene for osteoporosis in the specific populations and its role in the development of Gaucher disease.
Wang CH, Huang YN, Liao WL, Hsieh AR, Lin WD, Liu KW, Lu WL, Huang CC, Chien YH, Lee NC, et al. Orphanet J Rare Dis. 2024 Apr 4; 19(1):144. Epub 2024 Apr 4.
Peripheral Upregulation of Parkinson's Disease-Associated Genes Encoding α-Synuclein, β-Glucocerebrosidase, and Ceramide Glucosyltransferase in Major Depression. [Int J Mol Sci. 2024]
Peripheral Upregulation of Parkinson's Disease-Associated Genes Encoding α-Synuclein, β-Glucocerebrosidase, and Ceramide Glucosyltransferase in Major Depression.
Brazdis RM, von Zimmermann C, Lenz B, Kornhuber J, Mühle C. Int J Mol Sci. 2024 Mar 12; 25(6). Epub 2024 Mar 12.

RefSeq alternative splicing
See 5 reference mRNA sequence splice variants for the GBA1 gene.
RefSeq protein product
See the reference protein sequence for lysosomal acid glucosylceramidase isoform 2 (NP_001165282.1).

Protein
Protein sequence from Nucleotide coding region
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Nucleotide