Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4247
Gene name Gene Name - the full gene name approved by the HGNC.
Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MGAT2
Synonyms (NCBI Gene) Gene synonyms aliases
CDG2A, CDGS2, GLCNACTII, GNT-II, GNT2
Disease Acronyms (UniProt) Disease acronyms from UniProt database
CDG2A
Chromosome Chromosome number
14
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
14q21.3
Summary Summary of gene provided in NCBI Entrez Gene.
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 sign
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT047885 hsa-miR-30c-5p CLASH 23622248
MIRT1146871 hsa-miR-188-5p CLIP-seq
MIRT1146872 hsa-miR-200b CLIP-seq
MIRT1146873 hsa-miR-200c CLIP-seq
MIRT1146874 hsa-miR-3065-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IBA 21873635
GO:0000139 Component Golgi membrane IDA 20378551
GO:0000139 Component Golgi membrane TAS
GO:0005794 Component Golgi apparatus IDA
GO:0005795 Component Golgi stack IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
602616 7045 ENSG00000168282
Protein
UniProt ID Q10469
Protein name Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase (EC 2.4.1.143) (Beta-1,2-N-acetylglucosaminyltransferase II) (GlcNAc-T II) (GNT-II) (Mannoside acetylglucosaminyltransferase 2) (N-glycosyl-oligosaccharide-glycoprotein N-acetylglucosa
Protein function Plays an essential role in protein N-glycosylation. Catalyzes the transfer of N-acetylglucosamine (GlcNAc) onto the free terminal mannose moiety in the core structure of the nascent N-linked glycan chain, giving rise to the second branch in comp
PDB 5VCM , 5VCR , 5VCS
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05060 MGAT2 92 440 N-acetylglucosaminyltransferase II (MGAT2) Family
Sequence
Sequence length 447
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  N-Glycan biosynthesis
Various types of N-glycan biosynthesis
Metabolic pathways
  Defective MGAT2 causes MGAT2-CDG (CDG-2a)
Reactions specific to the complex N-glycan synthesis pathway
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Antithrombin deficiency Antithrombin III Deficiency rs121909546, rs121909547, rs121909548, rs121909549, rs121909550, rs121909551, rs2227624, rs121909552, rs121909554, rs121909555, rs121909557, rs121909558, rs28929469, rs1572088837, rs121909560
View all (41 more)
Congenital disorder of glycosylation Congenital disorder of glycosylation type 2A, MGAT2-CDG rs121434387, rs1264383808, rs766244312, rs1555497568, rs1555496968, rs267606740, rs1568296260, rs1562937199, rs28939378, rs121908583, rs1568757730, rs28936415, rs587776874, rs387906831, rs151173406
View all (80 more)
8808595, 27604308, 11228641, 19419693
Developmental delay Global developmental delay rs28941770, rs199469464, rs281865469, rs143747297, rs398123009, rs587777428, rs786205133, rs606231459, rs797044854, rs797045027, rs864309504, rs878853160, rs886039902, rs886042046, rs886041291
View all (32 more)
Hearing loss Sensorineural Hearing Loss (disorder) rs267607135, rs267606855, rs779841884, rs267606854, rs28942097, rs121908073, rs121908076, rs74315289, rs121908144, rs111033313, rs74315437, rs121908348, rs121908349, rs121908350, rs397515359
View all (184 more)
Associations from Text Mining
Disease Name Relationship Type References
Agammaglobulinemia Associate 33044030
Congenital disorder of glycosylation type 2A Associate 8808595
Congenital Disorders of Glycosylation Associate 29869806, 33044030
Developmental Disabilities Associate 33044030
Diabetes Gestational Inhibit 24262292
Epilepsy Associate 33044030
Genetic Diseases Inborn Associate 7607254, 8808595
Heart Arrest Associate 33044030
Immune System Diseases Associate 33044030
Muscle Hypotonia Associate 33044030