Entity Details

Primary name ST3GAL5
Entity type gene
Source Source Link

Details

PrimaryID8869
RefseqGeneNG_012807
SymbolST3GAL5
NameST3 beta-galactoside alpha-2,3-sialyltransferase 5
Chromosome2
Location2p11.2
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1999-06-15
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsSIAT9_HUMAN

GO terms

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GOName
GO:0000139 Golgi membrane
GO:0001574 ganglioside biosynthetic process
GO:0004513 neolactotetraosylceramide alpha-2,3-sialyltransferase activity
GO:0005887 integral component of plasma membrane
GO:0005975 carbohydrate metabolic process
GO:0006486 protein glycosylation
GO:0006688 glycosphingolipid biosynthetic process
GO:0008373 sialyltransferase activity
GO:0016021 integral component of membrane
GO:0047291 lactosylceramide alpha-2,3-sialyltransferase activity

Diseases

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Disease IDSourceNameDescription
609056 OMIMSalt and pepper developmental regression syndrome (SPDRS)A rare autosomal recessive disorder characterized by infantile onset of severe, recurrent and refractory seizures, failure to thrive, psychomotor delay, developmental stagnation, and cortical blindness. Deafness is observed in some patients. Affected individuals have patches of skin hypo- or hyperpigmentation on the trunk, face, and extremities. The disease is caused by variants affecting the gene represented in this entry.

Interactions

4 interactions

InteractorPartnerSourcesPublicationsLink
ST3GAL5BIN1IntAct31413325 details
ST3GAL5NDUFAF7BioGRID, IntAct26186194 28514442 details
ST3GAL5TMEM259BioGRID, IntAct26186194 28514442 details
ST3GAL5HLA-DPB1BioGRID26186194 details