Alpha-1,6-Mannosyl-Glycoprotein Beta-1,2-N-Acetylglucosaminyltransferase

Alternative Names

  • MGAT2
  • GlcNac-T II
  • GnT II
  • GnT2
  • UDP-N-Acetylglucosamine:Alpha-6-D-Mannoside Beta-1,2-N-Acetylglucosaminyltransferase II
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OMIM Number

602616

NCBI Gene ID

4247

Uniprot ID

Q10469

Length

2,683 bases

No. of Exons

1

No. of isoforms

1

Protein Name

Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase

Molecular Mass

51550 Da

Amino Acid Count

447

Genomic Location

chr14:49,620,798-49,623,480

Gene Map Locus
14q21.3

Description

The product of this gene is a Golgi enzyme catalyzing an essential step in the conversion of oligomannose to complex N-glycans. The enzyme has the typical glycosyltransferase domains: a short N-terminal cytoplasmic domain, a hydrophobic non-cleavable signal-anchor domain, and a C-terminal catalytic domain. Mutations in this gene may lead to carbohydrate-deficient glycoprotein syndrome, type II. The coding region of this gene is intronless. Transcript variants with a spliced 5' UTR may exist, but their biological validity has not been determined. [From RefSeq]

Epidemiology in the Arab World

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Variant NameCountryGenomic LocationClinvar Clinical SignificanceCTGA Clinical Significance Condition(s)HGVS ExpressionsdbSNPClinvar
NM_002408.3:c.693delLebanonNC_000014.9:g.49621961delLikely PathogenicCongenital Disorder Of Glycosylation, Type IIaNG_033054.1:g.3673del; NM_002408.3:c.693del; NP_002399.1:p.Lys231AsnfsTer15
NM_002408.3:c.711G>CSaudi ArabiaNC_000014.9:g.49621979G>CLikely Pathogenic, PathogenicPathogenicCongenital Disorder Of Glycosylation, Type IIaNG_033054.1:g.3653C>G; NM_002408.3:c.711G>C; NP_002399.1:p.Lys237Asn73088221830270
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