LIPID MAPSĀ® Gene/Proteome Database (LMPD)

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LMPD Record

LMP013516

Gene Information

Entrez Gene ID364675
Gene Namexylosylprotein beta 1,4-galactosyltransferase, polypeptide 7
Gene SymbolB4galt7
SpeciesRattus norvegicus
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0005794 ISS:UniProtKBCGolgi apparatus
GO:0016021 ISS:UniProtKBCintegral component of membrane
GO:0003831 IEA:EnsemblFbeta-N-acetylglucosaminylglycopeptide beta-1,4-galactosyltransferase activity
GO:0008378 ISS:UniProtKBFgalactosyltransferase activity
GO:0030145 IEA:EnsemblFmanganese ion binding
GO:0046525 ISS:UniProtKBFxylosylprotein 4-beta-galactosyltransferase activity
GO:0043206 ISS:UniProtKBPextracellular fibril organization
GO:0006024 ISS:UniProtKBPglycosaminoglycan biosynthetic process
GO:0048147 ISS:UniProtKBPnegative regulation of fibroblast proliferation
GO:0006487 IEA:EnsemblPprotein N-linked glycosylation
GO:0006029 ISS:UniProtKBPproteoglycan metabolic process
KEGG Pathway Links
KEGG Pathway IDDescription
ko00532Glycosaminoglycan biosynthesis - chondroitin sulfate / dermatan sulfate
rno00532Glycosaminoglycan biosynthesis - chondroitin sulfate / dermatan sulfate
ko00534Glycosaminoglycan biosynthesis - heparan sulfate / heparin
rno00534Glycosaminoglycan biosynthesis - heparan sulfate / heparin
M00057Glycosaminoglycan biosynthesis, linkage tetrasaccharide
rno01100Metabolic pathways
REACTOME Pathway Links
REACTOME Pathway IDDescription
5954521A tetrasaccharide linker sequence is required for GAG synthesis
5954488Chondroitin sulfate/dermatan sulfate metabolism
5953253Disease
5953252Glycogen storage diseases
5953861Glycosaminoglycan metabolism
5954347Heparan sulfate/heparin (HS-GAG) metabolism
5953250Metabolism
5953249Metabolism of carbohydrates
5953870MPS I - Hurler syndrome
5953869MPS II - Hunter syndrome
5953872MPS IIIA - Sanfilippo syndrome A
5953864MPS IIIB - Sanfilippo syndrome B
5953867MPS IIIC - Sanfilippo syndrome C
5953871MPS IIID - Sanfilippo syndrome D
5953866MPS IV - Morquio syndrome A
5953873MPS IV - Morquio syndrome B
5953862MPS IX - Natowicz syndrome
5953868MPS VII - Sly syndrome
5953865MPS VI - Maroteaux-Lamy syndrome
5953863Mucopolysaccharidoses
5953251Myoclonic epilepsy of Lafora