MGP Database

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MGP003865

Ontology/Pathway Information

Entrez Gene ID9331
Gene NameUDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 6
Gene Symbol B4GALT6
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0032580 IEA:UniProtKB-SubCellCGolgi cisterna membrane
GO:0000139 TAS:ReactomeCGolgi membrane
GO:0016021 IEA:UniProtKB-KWCintegral component of membrane
GO:0008378 TAS:ProtIncFgalactosyltransferase activity
GO:0046872 IEA:UniProtKB-KWFmetal ion binding
GO:0005975 TAS:ReactomePcarbohydrate metabolic process
GO:0044267 TAS:ReactomePcellular protein metabolic process
GO:0030203 TAS:ReactomePglycosaminoglycan metabolic process
GO:0018146 TAS:ReactomePkeratan sulfate biosynthetic process
GO:0042339 TAS:ReactomePkeratan sulfate metabolic process
GO:0043687 TAS:ReactomePpost-translational protein modification
GO:0018279 TAS:ReactomePprotein N-linked glycosylation via asparagine
GO:0044281 TAS:ReactomePsmall molecule metabolic process
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_22426Asparagine N-linked glycosylation
REACT_268132Defective ALG11 causes ALG11-CDG (CDG-1p)
REACT_267773Defective ALG12 causes ALG12-CDG (CDG-1g)
REACT_268645Defective ALG14 causes congenital myasthenic syndrome (ALG14-CMS)
REACT_268144Defective ALG1 causes ALG1-CDG (CDG-1k)
REACT_268833Defective ALG2 causes ALG2-CDG (CDG-1i)
REACT_268185Defective ALG3 causes ALG3-CDG (CDG-1d)
REACT_267765Defective ALG6 causes ALG6-CDG (CDG-1c)
REACT_268459Defective ALG8 causes ALG8-CDG (CDG-1h)
REACT_268015Defective ALG9 causes ALG9-CDG (CDG-1l)
REACT_268678Defective B3GAT3 causes JDSSDHD
REACT_268431Defective B4GALT1 causes B4GALT1-CDG (CDG-2d)
REACT_268438Defective B4GALT1 causes B4GALT1-CDG (CDG-2d)
REACT_268749Defective B4GALT7 causes EDS, progeroid type
REACT_267917Defective CHST14 causes EDS, musculocontractural type
REACT_267648Defective CHST3 causes SEDCJD
REACT_268786Defective CHST6 causes MCDC1
REACT_268113Defective CHSY1 causes TPBS
REACT_268849Defective DPAGT1 causes DPAGT1-CDG (CDG-1j) and CMSTA2
REACT_267942Defective EXT1 causes exostoses 1, TRPS2 and CHDS
REACT_267741Defective EXT2 causes exostoses 2
REACT_268813Defective MAN1B1 causes MRT15
REACT_268600Defective MGAT2 causes MGAT2-CDG (CDG-2a)
REACT_267905Defective MOGS causes MOGS-CDG (CDG-2b)
REACT_268619Defective MPDU1 causes MPDU1-CDG (CDG-1f)
REACT_268843Defective PAPSS2 causes SEMD-PA
REACT_268458Defective RFT1 causes RFT1-CDG (CDG-1n)
REACT_268059Defective SLC26A2 causes chondrodysplasias
REACT_116125Disease
REACT_268624Diseases associated with glycosaminoglycan metabolism
REACT_267875Diseases associated with N-glycosylation of proteins
REACT_268324Diseases of glycosylation
REACT_264090Glycogen storage diseases
REACT_121315Glycosaminoglycan metabolism
REACT_121120Keratan sulfate biosynthesis
REACT_121288Keratan sulfate/keratin metabolism
REACT_111217Metabolism
REACT_474Metabolism of carbohydrates
REACT_17015Metabolism of proteins
REACT_147857MPS I - Hurler syndrome
REACT_147734MPS II - Hunter syndrome
REACT_147753MPS IIIA - Sanfilippo syndrome A
REACT_147788MPS IIIB - Sanfilippo syndrome B
REACT_147860MPS IIIC - Sanfilippo syndrome C
REACT_147749MPS IIID - Sanfilippo syndrome D
REACT_147825MPS IV - Morquio syndrome A
REACT_147798MPS IV - Morquio syndrome B
REACT_147739MPS IX - Natowicz syndrome
REACT_147759MPS VII - Sly syndrome
REACT_147719MPS VI - Maroteaux-Lamy syndrome
REACT_147853Mucopolysaccharidoses
REACT_264430Myoclonic epilepsy of Lafora
REACT_25085N-Glycan antennae elongation
REACT_25208N-glycan antennae elongation in the medial/trans-Golgi
REACT_263902O-linked glycosylation
REACT_115606O-linked glycosylation of mucins
REACT_22161Post-translational protein modification
REACT_25046Transport to the Golgi and subsequent modification
SMP Pathway Links
SMP IDDescription
SMP00525Fabry disease
SMP00349Gaucher Disease
SMP00348Globoid Cell Leukodystrophy
SMP00526Krabbe disease
SMP00347Metachromatic Leukodystrophy (MLD)
SMP00034Sphingolipid Metabolism
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