Homo sapiens ST3 beta-galactoside alpha-2,3-sialyltransferase 5 (ST3GA - Nucleotide

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Neural-specific alterations in glycosphingolipid biosynthesis and cell signaling associated with two human ganglioside GM3 synthase deficiency variants. [Hum Mol Genet. 2023]
Neural-specific alterations in glycosphingolipid biosynthesis and cell signaling associated with two human ganglioside GM3 synthase deficiency variants.
Dookwah M, Wagner SK, Ishihara M, Yu SH, Ulrichs H, Kulik MJ, Zeltner N, Dalton S, Strauss KA, Aoki K, et al. Hum Mol Genet. 2023 Dec 1; 32(24):3323-3341.
GM3 Synthase Deficiency. [GeneReviews(®). 1993]
GM3 Synthase Deficiency.
Cruz V, Xin B, Wang H. GeneReviews(®). 1993-2024. 2023 Jul 20
Neurological insights on two siblings with GM3 synthase deficiency due to novel compound heterozygous ST3GAL5 variants. [Brain Dev. 2023]
Neurological insights on two siblings with GM3 synthase deficiency due to novel compound heterozygous ST3GAL5 variants.
Watanabe S, Lei M, Nakagawa E, Takeshita E, Inamori KI, Shishido F, Sasaki M, Mitsuhashi S, Matsumoto N, Kimura Y, et al. Brain Dev. 2023 May; 45(5):270-277. Epub 2023 Jan 21.

RefSeq protein product
See the reference protein sequence for lactosylceramide alpha-2,3-sialyltransferase isoform 3 (NP_001341163.1).

Protein
Protein sequence from Nucleotide coding region
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Homo sapiens ST3 beta-galactoside alpha-2,3-sialyltransferase 5 (ST3GAL5), trans...
Homo sapiens ST3 beta-galactoside alpha-2,3-sialyltransferase 5 (ST3GAL5), transcript variant 9, mRNA
gi|1229385559|ref|NM_001354234.1|

Nucleotide

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Nucleotide