Homo sapiens Gene: MGAT2 | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Gene | IDBG-5731.6 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | MGAT2 | ||||||||||||||||||
Gene Name | mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase | ||||||||||||||||||
Synonyms | CDG2A; CDGS2; GLCNACTII; GNT-II; GNT2 | ||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Gene | ENSG00000168282 | ||||||||||||||||||
Encoded Proteins |
mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase
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Protein Structure |
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Useful resources | Stemformatics EHFPI ImmGen | ||||||||||||||||||
Entrez Gene | |||||||||||||||||||
Summary |
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. [provided by RefSeq, Jul 2008] 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. [provided by RefSeq, Jul 2008] |
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Gene Information | |||||||||||||||||||
Type | Protein coding | ||||||||||||||||||
Genomic Location | Chromosome 14:49620795-49623481 | ||||||||||||||||||
Strand | Forward strand | ||||||||||||||||||
Band | q21.3 | ||||||||||||||||||
Transcripts |
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Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 4 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||||||||||||||
Species
Mus musculus
Bos taurus
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Gene ID
Gene Order
Not yet available
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Pathways | |||||||||||||||||||
NETPATH | |||||||||||||||||||
REACTOME |
Reactions specific to the complex N-glycan synthesis pathway pathway
Transport to the Golgi and subsequent modification pathway
Asparagine N-linked glycosylation pathway
Post-translational protein modification pathway
N-glycan antennae elongation in the medial/trans-Golgi pathway
Metabolism of proteins pathway
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KEGG |
N-Glycan biosynthesis pathway
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INOH | |||||||||||||||||||
PID NCI | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | Q10469 | ||||||||||||||||||
TrEMBL | B4DDK9 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 4247 | ||||||||||||||||||
UniGene | Hs.93338 | ||||||||||||||||||
RefSeq | NM_002408 | ||||||||||||||||||
HUGO | HGNC:7045 | ||||||||||||||||||
OMIM | 602616 | ||||||||||||||||||
CCDS | CCDS9690 | ||||||||||||||||||
HPRD | |||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AK056167 AK075199 AK293231 BC006390 CH471078 U15128 | ||||||||||||||||||
GenPept | AAA86956 AAH06390 BAG51637 BAG52082 BAG56770 EAW65758 | ||||||||||||||||||
RNA Seq Atlas | 4247 | ||||||||||||||||||