Gene Gene information from NCBI Gene database.
Entrez ID 85365
Gene name ALG2 alpha-1,3/1,6-mannosyltransferase
Gene symbol ALG2
Synonyms (NCBI Gene)
CDG1ICDGIiCMS14CMSTA3NET38hALPG2
Chromosome 9
Chromosome location 9q22.33
Summary This gene encodes a member of the glycosyltransferase 1 family. The encoded protein acts as an alpha 1,3 mannosyltransferase, mannosylating Man(2)GlcNAc(2)-dolichol diphosphate and Man(1)GlcNAc(2)-dolichol diphosphate to form Man(3)GlcNAc(2)-dolichol diph
SNPs SNP information provided by dbSNP.
2
SNP ID Visualize variation Clinical significance Consequence
rs387906281 C>- Pathogenic Non coding transcript variant, frameshift variant, coding sequence variant
rs730880304 C>A,T Pathogenic Missense variant, non coding transcript variant, coding sequence variant, synonymous variant
miRNA miRNA information provided by mirtarbase database.
252
miRTarBase ID miRNA Experiments Reference
MIRT023051 hsa-miR-124-3p Microarray 18668037
MIRT023983 hsa-miR-1-3p Proteomics 18668040
MIRT027167 hsa-miR-103a-3p Sequencing 20371350
MIRT031276 hsa-miR-19b-3p Sequencing 20371350
MIRT031868 hsa-miR-16-5p Proteomics 18668040
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
24
GO ID Ontology Definition Evidence Reference
GO:0000033 Function Alpha-1,3-mannosyltransferase activity IBA
GO:0000033 Function Alpha-1,3-mannosyltransferase activity IDA 35136180
GO:0000033 Function Alpha-1,3-mannosyltransferase activity TAS
GO:0004378 Function GDP-Man:Man(1)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase activity IDA 12684507, 35136180
GO:0004378 Function GDP-Man:Man(1)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
607905 23159 ENSG00000119523
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9H553
Protein name Alpha-1,3/1,6-mannosyltransferase ALG2 (EC 2.4.1.132) (EC 2.4.1.257) (Asparagine-linked glycosylation protein 2 homolog) (GDP-Man:Man(1)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase) (GDP-Man:Man(1)GlcNAc(2)-PP-dolichol mannosyltransferase) (GDP-Man:Man(
Protein function Mannosyltransferase that operates in the biosynthetic pathway of dolichol-linked oligosaccharides, the glycan precursors employed in protein asparagine (N)-glycosylation. The assembly of dolichol-linked oligosaccharides begins on the cytosolic s
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13439 Glyco_transf_4 26 206 Glycosyltransferase Family 4 Domain
PF00534 Glycos_transf_1 211 393 Glycosyl transferases group 1 Family
Sequence
Sequence length 416
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
  Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein
Defective ALG2 causes ALG2-CDG (CDG-1i)
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
597
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
ALG2-congenital disorder of glycosylation Likely pathogenic; Pathogenic rs757068626, rs201729325, rs387906281, rs730880304, rs2490391562, rs1828806280 RCV001542584
RCV004565246
RCV001060196
RCV004562185
RCV003988727
RCV001169926
Congenital myasthenic syndrome 14 Likely pathogenic; Pathogenic rs387906281, rs730882123, rs730882051, rs1828723159, rs1828806340 RCV001060196
RCV000161140
RCV000161141
RCV003222591
RCV001280688
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
ALG2-related disorder Likely benign; Benign; Conflicting classifications of pathogenicity rs201667181, rs755793459, rs180849348, rs767971393, rs373175237, rs372679579, rs146770430, rs542863968, rs748947069, rs368075764, rs764916897 RCV003913675
RCV003933666
RCV003907437
RCV003984326
RCV003963903
RCV003956866
RCV003912763
RCV003942424
RCV004758035
RCV003942791
RCV003965353
Congenital disorder of glycosylation Uncertain significance rs544873504, rs886063259, rs139943534 RCV000317197
RCV000379953
RCV000265648
See cases Conflicting classifications of pathogenicity; Uncertain significance rs146770430, rs1054683823 RCV002252128
RCV002252247
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Attention Deficit Disorder with Hyperactivity Associate 30529763
Congenital disorder of glycosylation type II Associate 30776362
Congenital Disorder Of Glycosylation Type Im Associate 12684507
Congenital Disorders of Glycosylation Associate 33644825
Epilepsy Idiopathic Generalized Associate 33503978
Genetic Diseases Inborn Associate 33644825
Glycogen Storage Disease XIV Associate 35279850, 38256263
Lung Neoplasms Stimulate 19383317
Malignant mesenchymal tumor Stimulate 19383317
Melanoma Associate 15366927