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ALG3 - Revision history
2024-03-29T01:52:49Z
Revision history for this page on the wiki
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https://www.wikidoc.org/index.php?title=ALG3&diff=1532386&oldid=prev
imported>Sherbruik at 11:11, 14 November 2018
2018-11-14T11:11:07Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 11:11, 14 November 2018</td>
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<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del style="font-weight: bold; text-decoration: none;">{{Underlinked|date=February 2017}}</del></div></td><td colspan="2" class="diff-side-added"></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{Infobox_gene}}</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{Infobox_gene}}</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>'''Dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichyl mannosyltransferase''' is an [[enzyme]] that in humans is encoded by the ''ALG3'' [[gene]].<ref name="pmid1058125">{{cite journal | author = Jerrold LE | title = Will an electric current replace the syringe for anesthesia? | journal = Dent Stud | volume = 53 | issue = 5 | pages = 49, 54 |date=Dec 1975 | pmid = 1058125 | pmc = | doi = }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: ALG3 asparagine-linked glycosylation 3 homolog (S. cerevisiae, alpha-1,3-mannosyltransferase)| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=10195| accessdate = }}</ref></div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>'''Dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichyl mannosyltransferase''' is an [[enzyme]] that<ins style="font-weight: bold; text-decoration: none;">, </ins>in humans<ins style="font-weight: bold; text-decoration: none;">, </ins>is encoded by the ''ALG3'' [[gene]].<ref name="pmid1058125">{{cite journal | author = Jerrold LE | title = Will an electric current replace the syringe for anesthesia? | journal = Dent Stud | volume = 53 | issue = 5 | pages = 49, 54 |date=Dec 1975 | pmid = 1058125 | pmc = | doi = }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: ALG3 asparagine-linked glycosylation 3 homolog (S. cerevisiae, alpha-1,3-mannosyltransferase)| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=10195| accessdate = }}</ref></div></td></tr>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div><!-- The PBB_Summary template is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. --></div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div><!-- The PBB_Summary template is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. --></div></td></tr>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| section_title = </div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>| section_title = </div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>| summary_text = This gene encodes a member of the ALG3 family. The encoded <del style="font-weight: bold; text-decoration: none;">protein </del>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.<ref name="entrez"/></div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>| summary_text = This gene encodes a member of the ALG3 family. The encoded <ins style="font-weight: bold; text-decoration: none;">[[wikt:protei|protei]]n </ins>catalyses the addition of the first <ins style="font-weight: bold; text-decoration: none;">[[</ins>dol-P-Man<ins style="font-weight: bold; text-decoration: none;">]] </ins>derived <ins style="font-weight: bold; text-decoration: none;">[[</ins>mannose<ins style="font-weight: bold; text-decoration: none;">]] </ins>in an alpha 1,3 linkage to Man5GlcNAc2-PP-Dol. Defects in this gene have been associated with <ins style="font-weight: bold; text-decoration: none;">[[</ins>congenital disorder<ins style="font-weight: bold; text-decoration: none;">]] </ins>of <ins style="font-weight: bold; text-decoration: none;">[[</ins>glycosylation<ins style="font-weight: bold; text-decoration: none;">]] </ins>type Id (CDG-Id) characterized by abnormal <ins style="font-weight: bold; text-decoration: none;">[[</ins>N-glycosylation<ins style="font-weight: bold; text-decoration: none;">]]</ins>.<ref name="entrez"/></div></td></tr>
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imported>Sherbruik
https://www.wikidoc.org/index.php?title=ALG3&diff=1413299&oldid=prev
en>KolbertBot: Bot: HTTP→HTTPS
2017-08-29T17:58:07Z
<p>Bot: <a href="/index.php?title=Wikipedia:Bots/Requests_for_approval/KolbertBot&action=edit&redlink=1" class="new" title="Wikipedia:Bots/Requests for approval/KolbertBot (page does not exist)">HTTP→HTTPS</a></p>
<p><b>New page</b></p><div>{{Underlinked|date=February 2017}}<br />
{{Infobox_gene}}<br />
'''Dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichyl mannosyltransferase''' is an [[enzyme]] that in humans is encoded by the ''ALG3'' [[gene]].<ref name="pmid1058125">{{cite journal | author = Jerrold LE | title = Will an electric current replace the syringe for anesthesia? | journal = Dent Stud | volume = 53 | issue = 5 | pages = 49, 54 |date=Dec 1975 | pmid = 1058125 | pmc = | doi = }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: ALG3 asparagine-linked glycosylation 3 homolog (S. cerevisiae, alpha-1,3-mannosyltransferase)| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=10195| accessdate = }}</ref><br />
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| section_title = <br />
| 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.<ref name="entrez"/><br />
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==References==<br />
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==Further reading==<br />
{{refbegin | 2}}<br />
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| citations = <br />
*{{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=10.1023/B:BOLI.0000031221.44647.9e }}<br />
*{{cite journal | vauthors=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=10.1097/01.mop.0000133636.56790.4a }}<br />
*{{cite journal | vauthors=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=10.1055/s-2007-979762 }}<br />
*{{cite journal | vauthors=Strausberg RL, Feingold EA, Grouse LH |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 | pmc=139241 |display-authors=etal}}<br />
*{{cite journal | vauthors=Denecke J, Kranz C, Kemming D |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 |display-authors=etal}}<br />
*{{cite journal | vauthors=Gerhard DS, Wagner L, Feingold EA |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 | pmc=528928 |display-authors=etal}}<br />
*{{cite journal | vauthors=Denecke J, Kranz C, ((von Kleist-Retzow JCh)) |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.B6 |display-authors=etal}}<br />
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{{refend}}<br />
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==External links==<br />
* [https://www.ncbi.nlm.nih.gov/books/NBK1332/ GeneReviews/NCBI/NIH/UW entry on Congenital Disorders of Glycosylation Overview]<br />
* {{UCSC genome browser|ALG3}}<br />
* {{UCSC gene details|ALG3}}<br />
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en>KolbertBot