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ALG6 alpha-1,3-glucosyltransferase

Summary

Gene Symbol

ALG6

Aliases

dolichyl-P-Glc:Man(9)GlcNAc(2)-PP-dolichol alpha- 1->3-glucosyltransferase

Organism

Homo sapiens (human)

External Links

NCBI Gene

29929

GGDB ID

gg146

HGNC

23157

mRNA

NM_013339

map

1p31.3

Protein

NP_037471

OMIM

604566

KEGG Gene ID

hsa:29929

PubChem

29929

Alliance of Genome Resources

HGNC:23157

Annotation

Keyword

Congenital disorder of glycosylation
Disease variant
Endoplasmic reticulum
Glycoprotein
Glycosyltransferase
Reference proteome
Transmembrane helix

Proteins

Displaying 1 entry
UniProt	Protein Name
Q9Y672	Asparagine-linked glycosylation protein 6 homolog Dol-P-Glc:Man(9)GlcNAc(2)-PP-Dol alpha-1,3-glucosyltransferase Dolichyl-P-Glc:Man9GlcNAc2-PP-dolichyl glucosyltransferase

Annotation information from UniProt.

Gene Ontology (GO)

Displaying **all 3** entries
GO Term	Evidence Code	PMID
protein N-linked glycosylation	IBA IDA IMP	10359825 10924277 25792706
dolichol-linked oligosaccharide biosynthetic process	IMP TAS	10359825 25792706
oligosaccharide-lipid intermediate biosynthetic process	IBA

GO Hierarchy

biological process

metabolic process [inference]

nitrogen compound metabolic process [inference]

organonitrogen compound metabolic process [inference]

protein metabolic process [inference]

protein modification process [inference]

protein glycosylation [inference]

protein N-linked glycosylation

biosynthetic process [inference]

organic substance biosynthetic process [inference]

carbohydrate derivative biosynthetic process [inference]

oligosaccharide-lipid intermediate biosynthetic process

dolichol-linked oligosaccharide biosynthetic process

cellular metabolic process [inference]

cellular lipid metabolic process [inference]

oligosaccharide-lipid intermediate biosynthetic process

dolichol-linked oligosaccharide biosynthetic process

isoprenoid metabolic process [inference]

polyprenol metabolic process [inference]

dolichol metabolic process [inference]

dolichol-linked oligosaccharide biosynthetic process

primary metabolic process [inference]

lipid metabolic process [inference]

cellular lipid metabolic process [inference]

oligosaccharide-lipid intermediate biosynthetic process

dolichol-linked oligosaccharide biosynthetic process

isoprenoid metabolic process [inference]

polyprenol metabolic process [inference]

dolichol metabolic process [inference]

dolichol-linked oligosaccharide biosynthetic process

protein metabolic process [inference]

protein modification process [inference]

protein glycosylation [inference]

protein N-linked glycosylation

small molecule metabolic process [inference]

alcohol metabolic process [inference]

polyprenol metabolic process [inference]

dolichol metabolic process [inference]

dolichol-linked oligosaccharide biosynthetic process

glycosylation [inference]

macromolecule glycosylation [inference]

protein glycosylation [inference]

protein N-linked glycosylation

organic substance metabolic process [inference]

lipid metabolic process [inference]

cellular lipid metabolic process [inference]

oligosaccharide-lipid intermediate biosynthetic process

dolichol-linked oligosaccharide biosynthetic process

isoprenoid metabolic process [inference]

polyprenol metabolic process [inference]

dolichol metabolic process [inference]

dolichol-linked oligosaccharide biosynthetic process

macromolecule metabolic process [inference]

protein metabolic process [inference]

protein modification process [inference]

protein glycosylation [inference]

protein N-linked glycosylation

macromolecule modification [inference]

protein modification process [inference]

protein glycosylation [inference]

protein N-linked glycosylation

macromolecule glycosylation [inference]

protein glycosylation [inference]

protein N-linked glycosylation

carbohydrate derivative metabolic process [inference]

carbohydrate derivative biosynthetic process [inference]

oligosaccharide-lipid intermediate biosynthetic process

dolichol-linked oligosaccharide biosynthetic process

organonitrogen compound metabolic process [inference]

protein metabolic process [inference]

protein modification process [inference]

protein glycosylation [inference]

protein N-linked glycosylation

organic substance biosynthetic process [inference]

carbohydrate derivative biosynthetic process [inference]

oligosaccharide-lipid intermediate biosynthetic process

dolichol-linked oligosaccharide biosynthetic process

organic hydroxy compound metabolic process [inference]

alcohol metabolic process [inference]

polyprenol metabolic process [inference]

dolichol metabolic process [inference]

dolichol-linked oligosaccharide biosynthetic process

cellular process [inference]

cellular metabolic process [inference]

cellular lipid metabolic process [inference]

oligosaccharide-lipid intermediate biosynthetic process

dolichol-linked oligosaccharide biosynthetic process

isoprenoid metabolic process [inference]

polyprenol metabolic process [inference]

dolichol metabolic process [inference]

dolichol-linked oligosaccharide biosynthetic process

Displaying **all 3** entries
GO Term	Evidence Code	PMID
lumenal side of endoplasmic reticulum membrane	IC	10359825
endoplasmic reticulum membrane	IBA TAS
membrane	HDA	19946888

GO Hierarchy

cellular component

cellular anatomical entity [inference]

membrane

organelle membrane [inference]

endoplasmic reticulum membrane

side of membrane [inference]

lumenal side of membrane [inference]

lumenal side of endoplasmic reticulum membrane

Displaying **all 3** entries
GO Term	Evidence Code	PMID
glucosyltransferase activity	IDA	10359825
dolichyl-phosphate-glucose-glycolipid alpha-glucosyltransferase activity	TAS
dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase activity	IBA IGI IMP	10359825 25792706

GO Hierarchy

molecular function

catalytic activity [inference]

transferase activity [inference]

glycosyltransferase activity [inference]

hexosyltransferase activity [inference]

glucosyltransferase activity

Gene Ontology information from NCBI Gene and UniProt.

Human Protein Atlas

ENSG00000088035

Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.

Data available from v23.0.proteinatlas.org. Image credit: Human Protein Atlas

GlycoGene Database (GGDB)

GGDB ID

gg146

Gene Symbol

ALG6

Reactions

Displaying 1 entry
Donor	Acceptor	Product	Reference
Dol-P-Glc	G39578OU	G24620AI

Displaying 1 entry
Donor	Acceptor	Product	Reference
Dol-P-Glc	G39578OU	G24620AI

Orthologous Gene

Displaying **all 6** entries
Species	Protein	mRNA
Arabidopsis thaliana	NP_198662	NM_123207
Saccharomyces cerevisiae	CAA99190	Z74910
Rattus norvegicus	XP_342869	XM_342868
Drosophila melanogaster	NP_609393	NM_135549
Caenorhabditis elegans	NP_495685	NM_063284
Mus musculus	NP_848899	NM_178784

Disease

Disease Ontology

Displaying entries **1 - 10** of 14 in total

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DO ID	Disease Name	Source
DOID:0050570	congenital disorder of glycosylation type I	DisGeNET DisGeNET Alliance of Genome Resources
DOID:0080552	congenital disorder of glycosylation Ia	DisGeNET
DOID:0080555	congenital disorder of glycosylation Ic	Glyco-Disease Genes Database DisGeNET Alliance of Genome Resources
DOID:11832	visual epilepsy	DisGeNET
DOID:1826	epilepsy	DisGeNET DisGeNET
DOID:2451	protein S deficiency	DisGeNET
DOID:2452	thrombophilia	DisGeNET
DOID:3755	antithrombin III deficiency	DisGeNET
DOID:3756	protein C deficiency	DisGeNET
DOID:5212	congenital disorder of glycosylation	DisGeNET

The Human Phenotype Ontology

Displaying entries **11 - 20** of 40 in total

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HPO ID	HPO Term
HP:0001156	Brachydactyly
HP:0001250	Seizure
HP:0001251	Ataxia
HP:0001252	Hypotonia
HP:0001263	Global developmental delay
HP:0001284	Areflexia
HP:0001321	Cerebellar hypoplasia
HP:0001392	Abnormality of the liver
HP:0001508	Failure to thrive
HP:0001929	Reduced factor XI activity

Displaying **all 2** entries
Disease ID	Disease Name
ORPHA:79320	ALG6-congenital disorder of glycosylation 1C
OMIM:603147	ALG6-congenital disorder of glycosylation 1C

PubChem Disease

GHR Health Conditions

ALG6-congenital disorder of glycosylation

MedGen Diseases

ALG6-congenital disorder of glycosylation 1C

OMIM Phenotypes

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ic; CDG1C

KEGG Diseases

Congenital disorders of glycosylation type I

Gene-Disease-Co-Occurrences-in-Literature (PubChem)

LIPID MAPS Gene / Proteome Database

LMPD ID: LMP012356
Gene Name: ALG6, alpha-1,3-glucosyltransferase

Ortholog

Displaying entries **31 - 40** of 83 in total

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Species	Gene ID	Orthologous MAtrix
Pongo abelii	100174089	PONAB16486
Canis lupus familiaris	609974	CANLF15641
Vulpes vulpes	112926070	VULVU20202
Ailuropoda melanoleuca	100474628	AILME14327
Mustela putorius furo	101691756	MUSPF13973
Felis catus	101082423	FELCA21187
Panthera leo	122227472	PANLE10005
Tursiops truncatus	101338575	TURTR07867
Balaenoptera musculus	118896269	BALMU23150
Loxodonta africana	100667963	LOXAF13526

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GlycoPOST

UniCarb-DR

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Other Information

Tools

Search Tools

Summary

External Links

Annotation

GlycoGene Database (GGDB)

PubChem Disease

LIPID MAPS Gene / Proteome Database

International Collaboration

Acknowledgements