OMG (gene): Difference between revisions
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'''Oligodendrocyte-myelin glycoprotein''' is a [[protein]] that in humans is encoded by the ''OMG'' [[gene]].<ref name="pmid1899288">{{cite journal | vauthors = Viskochil D, Cawthon R, O'Connell P, Xu GF, Stevens J, Culver M, Carey J, White R | title = The gene encoding the oligodendrocyte-myelin glycoprotein is embedded within the neurofibromatosis type 1 gene | journal = Mol Cell Biol | volume = 11 | issue = 2 | pages = 906–12 |date=Mar 1991 | pmid = 1899288 | pmc = 359746 | doi = }}</ref><ref name="pmid2277079">{{cite journal | vauthors = Mikol DD, Alexakos MJ, Bayley CA, Lemons RS, Le Beau MM, Stefansson K | title = Structure and chromosomal localization of the gene for the oligodendrocyte-myelin glycoprotein | journal = J Cell Biol | volume = 111 | issue = 6 Pt 1 | pages = 2673–9 |date=Mar 1991 | pmid = 2277079 | pmc = 2116377 | doi =10.1083/jcb.111.6.2673 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: OMG oligodendrocyte myelin glycoprotein| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=4974| accessdate = }}</ref> | '''Oligodendrocyte-myelin glycoprotein''' is a [[protein]] that in humans is encoded by the ''OMG'' [[gene]].<ref name="pmid1899288">{{cite journal | vauthors = Viskochil D, Cawthon R, O'Connell P, Xu GF, Stevens J, Culver M, Carey J, White R | title = The gene encoding the oligodendrocyte-myelin glycoprotein is embedded within the neurofibromatosis type 1 gene | journal = Mol Cell Biol | volume = 11 | issue = 2 | pages = 906–12 |date=Mar 1991 | pmid = 1899288 | pmc = 359746 | doi = }}</ref><ref name="pmid2277079">{{cite journal | vauthors = Mikol DD, Alexakos MJ, Bayley CA, Lemons RS, Le Beau MM, Stefansson K | title = Structure and chromosomal localization of the gene for the oligodendrocyte-myelin glycoprotein | journal = J Cell Biol | volume = 111 | issue = 6 Pt 1 | pages = 2673–9 |date=Mar 1991 | pmid = 2277079 | pmc = 2116377 | doi =10.1083/jcb.111.6.2673 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: OMG oligodendrocyte myelin glycoprotein| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=4974| accessdate = }}</ref> | ||
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*{{cite journal |vauthors=Vourc'h P, Moreau T, Arbion F, etal |title=Oligodendrocyte myelin glycoprotein growth inhibition function requires its conserved leucine-rich repeat domain, not its glycosylphosphatidyl-inositol anchor |journal=J. Neurochem. |volume=85 |issue= 4 |pages= 889–97 |year= 2003 |pmid= 12716421 |doi=10.1046/j.1471-4159.2003.01764.x }} | *{{cite journal |vauthors=Vourc'h P, Moreau T, Arbion F, etal |title=Oligodendrocyte myelin glycoprotein growth inhibition function requires its conserved leucine-rich repeat domain, not its glycosylphosphatidyl-inositol anchor |journal=J. Neurochem. |volume=85 |issue= 4 |pages= 889–97 |year= 2003 |pmid= 12716421 |doi=10.1046/j.1471-4159.2003.01764.x }} | ||
*{{cite journal |vauthors=Gerhard DS, Wagner L, Feingold EA, etal |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 }} | *{{cite journal |vauthors=Gerhard DS, Wagner L, Feingold EA, etal |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 }} | ||
*{{cite journal |vauthors=Venturin M, Moncini S, Villa V, etal |title=Mutations and novel polymorphisms in coding regions and UTRs of CDK5R1 and OMG genes in patients with non-syndromic mental retardation |journal=Neurogenetics |volume=7 |issue= 1 |pages= 59–66 |year= 2007 |pmid= 16425041 |doi= 10.1007/s10048-005-0026-9 }} | *{{cite journal |vauthors=Venturin M, Moncini S, Villa V, etal |title=Mutations and novel polymorphisms in coding regions and UTRs of CDK5R1 and OMG genes in patients with non-syndromic mental retardation |journal=Neurogenetics |volume=7 |issue= 1 |pages= 59–66 |year= 2007 |pmid= 16425041 |doi= 10.1007/s10048-005-0026-9 |url=https://air.unimi.it/bitstream/2434/10108/2/10_Mutations%20and%20novel%20polymorphisms.pdf }} | ||
*{{cite journal |vauthors=Douglas J, Cilliers D, Coleman K, etal |title=Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth |journal=Nat. Genet. |volume=39 |issue= 8 |pages= 963–5 |year= 2007 |pmid= 17632510 |doi= 10.1038/ng2083 }} | *{{cite journal |vauthors=Douglas J, Cilliers D, Coleman K, etal |title=Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth |journal=Nat. Genet. |volume=39 |issue= 8 |pages= 963–5 |year= 2007 |pmid= 17632510 |doi= 10.1038/ng2083 }} | ||
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Latest revision as of 14:08, 9 June 2018
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Oligodendrocyte-myelin glycoprotein is a protein that in humans is encoded by the OMG gene.[1][2][3]
References
- ↑ Viskochil D, Cawthon R, O'Connell P, Xu GF, Stevens J, Culver M, Carey J, White R (Mar 1991). "The gene encoding the oligodendrocyte-myelin glycoprotein is embedded within the neurofibromatosis type 1 gene". Mol Cell Biol. 11 (2): 906–12. PMC 359746. PMID 1899288.
- ↑ Mikol DD, Alexakos MJ, Bayley CA, Lemons RS, Le Beau MM, Stefansson K (Mar 1991). "Structure and chromosomal localization of the gene for the oligodendrocyte-myelin glycoprotein". J Cell Biol. 111 (6 Pt 1): 2673–9. doi:10.1083/jcb.111.6.2673. PMC 2116377. PMID 2277079.
- ↑ "Entrez Gene: OMG oligodendrocyte myelin glycoprotein".
Further reading
- Mikol DD, Gulcher JR, Stefansson K (1990). "The oligodendrocyte-myelin glycoprotein belongs to a distinct family of proteins and contains the HNK-1 carbohydrate". J. Cell Biol. 110 (2): 471–9. doi:10.1083/jcb.110.2.471. PMC 2116011. PMID 1688857.
- Mikol DD, Stefansson K (1988). "A phosphatidylinositol-linked peanut agglutinin-binding glycoprotein in central nervous system myelin and on oligodendrocytes". J. Cell Biol. 106 (4): 1273–9. doi:10.1083/jcb.106.4.1273. PMC 2115011. PMID 3283151.
- Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
- Mikol DD, Rongnoparut P, Allwardt BA, et al. (1993). "The oligodendrocyte-myelin glycoprotein of mouse: primary structure and gene structure". Genomics. 17 (3): 604–10. doi:10.1006/geno.1993.1379. PMID 8244377.
- Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
- Wang KC, Koprivica V, Kim JA, et al. (2002). "Oligodendrocyte-myelin glycoprotein is a Nogo receptor ligand that inhibits neurite outgrowth". Nature. 417 (6892): 941–4. doi:10.1038/nature00867. PMID 12068310.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Vourc'h P, Moreau T, Arbion F, et al. (2003). "Oligodendrocyte myelin glycoprotein growth inhibition function requires its conserved leucine-rich repeat domain, not its glycosylphosphatidyl-inositol anchor". J. Neurochem. 85 (4): 889–97. doi:10.1046/j.1471-4159.2003.01764.x. PMID 12716421.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
- Venturin M, Moncini S, Villa V, et al. (2007). "Mutations and novel polymorphisms in coding regions and UTRs of CDK5R1 and OMG genes in patients with non-syndromic mental retardation" (PDF). Neurogenetics. 7 (1): 59–66. doi:10.1007/s10048-005-0026-9. PMID 16425041.
- Douglas J, Cilliers D, Coleman K, et al. (2007). "Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth". Nat. Genet. 39 (8): 963–5. doi:10.1038/ng2083. PMID 17632510.
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