help  | about  | cite  | software

Gene : ALG3 Homo sapiens

Name  ? ALG3 alpha-1,3- mannosyltransferase Cytological Location  3q27.1
Brief Description  ALG3 alpha-1,3- mannosyltransferase
Description  This gene encodes a member of the ALG3 family. The encoded protein catalyses the addition of the first dol-P-Man derived mannose in an alpha 1,3 linkage to Man5GlcNAc2-PP-Dol. Defects in this gene have been associated with congenital disorder of glycosylation type Id (CDG-Id) characterized by abnormal N-glycosylation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2008]
  • synonyms:
  • HGNC:23056,
  • CDG1D,
  • CDGS4,
  • not,
  • BC002839,
  • asparagine-linked glycosylation 3 homolog (yeast, alpha-1,3-mannosyltransferase),
  • carbohydrate deficient glycoprotein syndrome type IV,
  • CDGS4,
  • D16Ertd36e,
  • D16Ertd36e,
  • ALG3,
  • uc003fne.3,
  • NM_005787,
  • Not56,
  • OTTHUMG00000156823,
  • CDGS6,
  • dol-P-Man dependent alpha-1,3- mannosyltransferase,
  • asparagine-linked glycosylation 3, alpha-1,3- mannosyltransferase homolog (S. cerevisiae),
  • Not56,
  • dol-P-Man:Man(5)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase,
  • NOT56L,
  • NOT56L
  • identifiers:
  • 10195,
  • ENSG00000214160,
  • ALG3

Genome feature

Region: gene ? Length: 16001  
Location: 3:184242301-184258301 reverse strand Cyto location: 3q27.1

Uni Prot Comments Displayer

Protein Atlas Displayer

Gene Expression Atlas Tissues Displayer

Gene Expression Atlas Diseases Displayer

Publication Counts Displayer

Curated Proteins Displayer


Gene Ontology Displayer

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


J Browse Displayer

Gene Structure Displayer

Overlapping Features Displayer

Mouse Alleles Displayer

Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


Homologue Displayer


Cytoscape Network Displayer

Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



214 SNPs

5 Cross References

18 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results