- ALG3
Asparagine-linked glycosylation 3 homolog (S. cerevisiae, alpha-1,3-mannosyltransferase), also known as ALG3, is a human
gene .cite web | title = Entrez Gene: ALG3 asparagine-linked glycosylation 3 homolog (S. cerevisiae, alpha-1,3-mannosyltransferase)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=10195| accessdate = ]PBB_Summary
section_title =
summary_text = 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.cite web | title = Entrez Gene: ALG3 asparagine-linked glycosylation 3 homolog (S. cerevisiae, alpha-1,3-mannosyltransferase)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=10195| accessdate = ]References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Jaeken J |title=Congenital disorders of glycosylation (CDG): update and new developments. |journal=J. Inherit. Metab. Dis. |volume=27 |issue= 3 |pages= 423–6 |year= 2005 |pmid= 15272470 |doi=
*cite journal | author=Jaeken J, Carchon H |title=Congenital disorders of glycosylation: a booming chapter of pediatrics. |journal=Curr. Opin. Pediatr. |volume=16 |issue= 4 |pages= 434–9 |year= 2004 |pmid= 15273506 |doi=
*cite journal | author=Jerrold LE |title=Will an electric current replace the syringe for anesthesia? |journal=Dental student |volume=53 |issue= 5 |pages= 49, 54 |year= 1975 |pmid= 1058125 |doi=
*cite journal | author=Stibler H, Stephani U, Kutsch U |title=Carbohydrate-deficient glycoprotein syndrome--a fourth subtype. |journal=Neuropediatrics |volume=26 |issue= 5 |pages= 235–7 |year= 1996 |pmid= 8552211 |doi=
*cite journal | author=Körner C, Knauer R, Stephani U, "et al." |title=Carbohydrate deficient glycoprotein syndrome type IV: deficiency of dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichyl mannosyltransferase. |journal=EMBO J. |volume=18 |issue= 23 |pages= 6816–22 |year= 2000 |pmid= 10581255 |doi= 10.1093/emboj/18.23.6816
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Denecke J, Kranz C, Kemming D, "et al." |title=An activated 5' cryptic splice site in the human ALG3 gene generates a premature termination codon insensitive to nonsense-mediated mRNA decay in a new case of congenital disorder of glycosylation type Id (CDG-Id). |journal=Hum. Mutat. |volume=23 |issue= 5 |pages= 477–86 |year= 2004 |pmid= 15108280 |doi= 10.1002/humu.20026
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Denecke J, Kranz C, von Kleist-Retzow JCh, "et al." |title=Congenital disorder of glycosylation type Id: clinical phenotype, molecular analysis, prenatal diagnosis, and glycosylation of fetal proteins. |journal=Pediatr. Res. |volume=58 |issue= 2 |pages= 248–53 |year= 2005 |pmid= 16006436 |doi= 10.1203/01.PDR.0000169963.94378.B6PBB_Controls
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