The protein encoded by this gene is a type II membrane protein that catalyzes the transfer of sialic acid from CMP-sialic acid to galactose-containing substrates. The encoded protein is normally found in the Golgi apparatus but can be proteolytically processed to a soluble form. This protein is a member of glycosyltransferase family 29. Mutations in this gene have been associated with a form of autosomal recessive nonsymdromic cognitive disability as well as infantile epileptic encephalopathy. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ST3GAL3-20-RE | 20 (40 μL) | 200 μL |  |
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| ST3GAL3-20-OR | 20 (40 μL) | 200 μL |  |
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| ST3GAL3-20-GO | 20 (40 μL) | 200 μL |  |
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| ST3GAL3-20-GR | 20 (40 μL) | 200 μL |  |
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| ST3GAL3-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is a type II membrane protein that catalyzes the transfer of sialic acid from CMP-sialic acid to galactose-containing substrates. The encoded protein is normally found in the Golgi apparatus but can be proteolytically processed to a soluble form. This protein is a member of glycosyltransferase family 29. Mutations in this gene have been associated with a form of autosomal recessive nonsymdromic cognitive disability as well as infantile epileptic encephalopathy. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]
Gene Symbol : ST3GAL3
Gene Name : ST3 beta-galactoside alpha-2,3-sialyltransferase 3
Chromosome : CHR 1: 437,074,96-439,311,64
Locus : 1p34.1
Alt. Genes : CLEC3A
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