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protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)

Summary

Gene Symbol

POMGNT2

Aliases

AGO61
FLJ14566
protein O-mannose beta-1,4-N-acetylglucosaminyltransferase 2

Organism

Homo sapiens (human)

External Links

NCBI Gene

84892

GGDB ID

gg235

HGNC

25902

mRNA

NM_032806

Protein

NP_116195

OMIM

614828

KEGG Gene ID

hsa:84892

PubChem

84892

Alliance of Genome Resources

HGNC:25902

Annotation

Keyword

3D-structure
Congenital muscular dystrophy
Disease variant
Dystroglycanopathy
Endoplasmic reticulum
Glycoprotein
Glycosyltransferase
Limb-girdle muscular dystrophy
Lissencephaly
Reference proteome
Signal-anchor
Transmembrane helix

Proteins

Displaying 1 entry
UniProt	Protein Name
Q8NAT1	Extracellular O-linked N-acetylglucosamine transferase-like Glycosyltransferase-like domain-containing protein 2

Annotation information from UniProt.

Gene Ontology (GO)

Displaying entries **1 - 5** of 6 in total

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GO Term	Evidence Code	PMID
neuron migration	ISS
protein O-linked glycosylation	TAS
protein O-linked glycosylation	IDA	23929950
protein O-linked glycosylation	IMP	27066570
protein O-linked mannosylation	ISS

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 O-linked glycosylation

protein O-linked mannosylation

protein mannosylation [inference]

protein O-linked mannosylation

primary metabolic process [inference]

protein metabolic process [inference]

protein modification process [inference]

protein glycosylation [inference]

protein O-linked glycosylation

protein O-linked mannosylation

protein mannosylation [inference]

protein O-linked mannosylation

glycosylation [inference]

macromolecule glycosylation [inference]

protein glycosylation [inference]

protein O-linked glycosylation

protein O-linked mannosylation

protein mannosylation [inference]

protein O-linked mannosylation

mannosylation [inference]

protein mannosylation [inference]

protein O-linked mannosylation

organic substance metabolic process [inference]

macromolecule metabolic process [inference]

protein metabolic process [inference]

protein modification process [inference]

protein glycosylation [inference]

protein O-linked glycosylation

protein O-linked mannosylation

protein mannosylation [inference]

protein O-linked mannosylation

macromolecule modification [inference]

protein modification process [inference]

protein glycosylation [inference]

protein O-linked glycosylation

protein O-linked mannosylation

protein mannosylation [inference]

protein O-linked mannosylation

macromolecule glycosylation [inference]

protein glycosylation [inference]

protein O-linked glycosylation

protein O-linked mannosylation

protein mannosylation [inference]

protein O-linked mannosylation

organonitrogen compound metabolic process [inference]

protein metabolic process [inference]

protein modification process [inference]

protein glycosylation [inference]

protein O-linked glycosylation

protein O-linked mannosylation

protein mannosylation [inference]

protein O-linked mannosylation

cellular process [inference]

cell motility [inference]

cell migration [inference]

neuron migration

Displaying **all 3** entries
GO Term	Evidence Code	PMID
endoplasmic reticulum	IDA	23929950 27066570
endoplasmic reticulum	IBA
endoplasmic reticulum membrane	TAS

GO Hierarchy

cellular component

cellular anatomical entity [inference]

membrane [inference]

organelle membrane [inference]

endoplasmic reticulum membrane

organelle [inference]

membrane-bounded organelle [inference]

intracellular membrane-bounded organelle [inference]

endoplasmic reticulum

intracellular organelle [inference]

intracellular membrane-bounded organelle [inference]

endoplasmic reticulum

Displaying entries **1 - 5** of 6 in total

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GO Term	Evidence Code	PMID
protein binding	IPI	25416956
acetylglucosaminyltransferase activity	TAS
acetylglucosaminyltransferase activity	IDA	23929950
protein O-acetylglucosaminyltransferase activity	IDA	23929950
protein O-acetylglucosaminyltransferase activity	IMP	27066570

GO Hierarchy

molecular function

catalytic activity [inference]

transferase activity [inference]

glycosyltransferase activity [inference]

UDP-glycosyltransferase activity [inference]

acetylglucosaminyltransferase activity

protein O-acetylglucosaminyltransferase activity

hexosyltransferase activity [inference]

acetylglucosaminyltransferase activity

protein O-acetylglucosaminyltransferase activity

catalytic activity, acting on a protein [inference]

protein O-acetylglucosaminyltransferase activity

binding [inference]

protein binding

Gene Ontology information from NCBI Gene and UniProt.

OrthoDB (Group)

Group level

Eukaryota

Group Name

EGF domain-specific O-linked N-acetylglucosamine transferase

Functional Category

D: Cell cycle control, cell division, chromosome partitioning
M: Cell wall/membrane/envelope biogenesis
O: Posttranslational modification, protein turnover, chaperones

Displaying 1 entry
Gene Ontology
transferase activity

Displaying **all 2** entries
InterPro
Glycosyltransferase 61, catalytic domain
Glycosyltransferase 61

GlycoGene Database (GGDB)

GGDB ID

gg235

Gene Symbol

POMGNT2

Reactions

Displaying 1 entry
Donor	Acceptor	Reducing terminal(Acceptor)	Product	Reducing terminal(Product)	Reference
UDP-GlcNAc	G61491DK	MU	G97041TX	MU	23929950

Displaying 1 entry
Donor	Acceptor	Reducing terminal(Acceptor)	Product	Reducing terminal(Product)	Reference
UDP-GlcNAc	G61491DK	MU	G97041TX	MU	23929950

KEGG BRITE Database

Orthology

K18207

Name

protein O-mannose beta-1,4-N-acetylglucosaminyltransferase [EC:2.4.1.312]

References

23929950

Rhea

RHEA:37663

UDP-N-acetyl-α-D-glucosamine

H⁺ + UDP

Enzyme

2.4.1.312

PMID

23929950

Disease

Disease Ontology

Displaying **all 2** entries
DO ID	Disease Name	Source
DOID:0111231	congenital muscular dystrophy-dystroglycanopathy type A8	Alliance of Genome Resources
DOID:0112382	muscular dystrophy-dystroglycanopathy type C8	Alliance of Genome Resources

The Human Phenotype Ontology

Displaying entries **41 - 50** of 60 in total

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HPO ID	HPO Term
HP:0002269	Abnormality of neuronal migration
HP:0002334	Abnormal cerebellar vermis morphology
HP:0002536	Abnormal cortical gyration
HP:0003202	Skeletal muscle atrophy
HP:0003236	Elevated circulating creatine kinase concentration
HP:0003391	Gowers sign
HP:0003560	Muscular dystrophy
HP:0003577	Congenital onset
HP:0003593	Infantile onset
HP:0003621	Juvenile onset

Displaying **all 3** entries
Disease ID	Disease Name
ORPHA:899	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4 muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7 muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1 muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A13 muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2 muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3 muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5 muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6 muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A9 muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11 muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8 muscular dystrophy-dystroglycanopathy, type A
OMIM:614830	muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8
OMIM:618135	muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8

PubChem Disease

MedGen Diseases

OMIM Phenotypes

KEGG Diseases

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

Ortholog

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Species	Gene ID	Alliance of Genome Resources	Orthologous MAtrix
Xenopus tropicalis	84892	Xenbase:XB-GENE-973748
Mus musculus	215494	Xenbase:XB-GENE-973748	MOUSE64227
Rattus norvegicus	316091	Xenbase:XB-GENE-973748	RATNO41852
Xenopus tropicalis	444520	Xenbase:XB-GENE-973748
Canis lupus familiaris	485621		CANLF09005
Xenopus tropicalis	496628	Xenbase:XB-GENE-973748
Bos taurus	497030		BOVIN17341
Danio rerio	497644	Xenbase:XB-GENE-973748	DANRE11595
Pan troglodytes	503649		PANTR30895
Macaca mulatta	717032		MACMU29377

GlyTouCan

GlyComb

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UniCarb-DR

LM-GlycoRepo

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Other Information

Tools

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Guidelines

Summary

External Links

Annotation

OrthoDB (Group)

GlycoGene Database (GGDB)

KEGG BRITE Database

PubChem Disease

International Collaboration

Acknowledgements