- Gene Overview
- Interaction Network
- Sequence Verification
ST3GAL3, ST3 beta-galactoside alpha-2,3-sialyltransferase 3
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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]
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Gene Synonyms (CMP-N-acetylneuraminate-beta-1,4-galactoside alpha-2,3-sialyltransferase, Gal beta-1,3(4)GlcNAc alpha-2,3 sialyltransferase, alpha 2,3-ST 3, alpha 2,3-sialyltransferase III, alpha-2,3-sialyltransferase II, sialyltransferase 6 (N-acetyllacosaminide alpha 2,3-sialyltransferase), sialyltransferase 6 (N-acetyllactosaminide alpha 2,3-sialyltransferase), EIEE15, MRT12, SIAT6, ST3GALII, ST3Gal III, ST3GalIII, ST3N,)
- NCBI Gene ID:
6487
- Species:
Homo sapiens (Human)
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UNIPROT ID#>>Q11203
- View the NCBI Database
for this Gene »
Gene products are often involved in multiple pathways and networks within a living
cell. Learn more about other interacting partners.
ST3 beta-galactoside alpha-2,3-sialyltransferase 3 interacts with:
Paste a protein or nucleic acid sequence in the box below to confirm that it matches
this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see
how a sequence matches to an experimentally-validated ORF clone.
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