CMP-N-acetylneuraminate-beta-1,4-galactoside alpha-2,3-sialyltransfera - Protein

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View conserved domains detected in this protein sequence using CD-search.
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Opens the Genome Data Viewer, NCBI's genome browser, at the genomic location at which this sequence is annotated. View this sequence in the context of other features annotated at the same location and browse to other genome regions.

The epilepsy phenotype of ST3GAL3-related developmental and epileptic encephalopathy. [Epilepsia Open. 2023]
The epilepsy phenotype of ST3GAL3-related developmental and epileptic encephalopathy.
Whitney R, Jain P, RamachandranNair R, Jones KC, Kiani H, Tarnopolsky M, Meaney B. Epilepsia Open. 2023 Jun; 8(2):623-632. Epub 2023 Apr 24.
ST3GAL3 Promotes the Inflammatory Response of Fibroblast-Like Synoviocytes in Rheumatoid Arthritis by Activating the TLR9/MyD88 Pathway. [Mediators Inflamm. 2022]
ST3GAL3 Promotes the Inflammatory Response of Fibroblast-Like Synoviocytes in Rheumatoid Arthritis by Activating the TLR9/MyD88 Pathway.
Xu L, Niu X, Liu Y, Liu L. Mediators Inflamm. 2022; 2022:4258742. Epub 2022 Nov 10.
A novel variant of ST3GAL3 causes non-syndromic autosomal recessive intellectual disability in Iranian patients. [J Gene Med. 2020]
A novel variant of ST3GAL3 causes non-syndromic autosomal recessive intellectual disability in Iranian patients.
Farajollahi Z, Razmara E, Heidari E, Jafarinia E, Garshasbi M. J Gene Med. 2020 Nov; 22(11):e3253. Epub 2020 Aug 3.

RefSeq mRNA
See reference mRNA sequence for the ST3GAL3 gene (XM_028834731.1).
RefSeq protein isoforms
See 15 reference sequence protein isoforms for the ST3GAL3 gene.

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Protein