(Redirected from
OPALIN (gene))
| OPALIN | |||||||||||||||||||||||||||||||||||||||||||||||||||
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| Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Aliases | OPALIN, HTMP10, TMEM10, TMP10, oligodendrocytic myelin paranodal and inner loop protein | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | OMIM: 617200; MGI: 2657025; HomoloGene: 13237; GeneCards: OPALIN; OMA: OPALIN - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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| Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Opalin is a protein that is encoded in humans by the OPALIN gene. [4] [5] [6]
References
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000050121 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ Nobile C, Hinzmann B, Scannapieco P, Siebert R, Zimbello R, Perez-Tur J, et al. (Jan 2002). "Identification and characterization of a novel human brain-specific gene, homologous to S. scrofa tmp83.5, in the chromosome 10q24 critical region for temporal lobe epilepsy and spastic paraplegia". Gene. 282 (1–2): 87–94. doi: 10.1016/S0378-1119(01)00846-0. PMID 11814680.
- ^ Aruga J, Yoshikawa F, Nozaki Y, Sakaki Y, Toyoda A, Furuichi T (Sep 2007). "An oligodendrocyte enhancer in a phylogenetically conserved intron region of the mammalian myelin gene Opalin". Journal of Neurochemistry. 102 (5): 1533–47. doi: 10.1111/j.1471-4159.2007.04583.x. PMID 17442045. S2CID 4231906.
- ^ "Entrez Gene: TMEM10 transmembrane protein 10".
Further reading
- Hartley JL, Temple GF, Brasch MA (Nov 2000). "DNA cloning using in vitro site-specific recombination". Genome Research. 10 (11): 1788–95. doi: 10.1101/gr.143000. PMC 310948. PMID 11076863.
- Simpson JC, Wellenreuther R, Poustka A, Pepperkok R, Wiemann S (Sep 2000). "Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing". EMBO Reports. 1 (3): 287–92. doi: 10.1093/embo-reports/kvd058. PMC 1083732. PMID 11256614.
- Wiemann S, Arlt D, Huber W, Wellenreuther R, Schleeger S, Mehrle A, Bechtel S, Sauermann M, Korf U, Pepperkok R, Sültmann H, Poustka A (Oct 2004). "From ORFeome to biology: a functional genomics pipeline". Genome Research. 14 (10B): 2136–44. doi: 10.1101/gr.2576704. PMC 528930. PMID 15489336.
 | This article on a gene on human chromosome 10 is a stub. You can help Wikipedia by expanding it. |
(Redirected from
OPALIN (gene))
| OPALIN | |||||||||||||||||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Aliases | OPALIN, HTMP10, TMEM10, TMP10, oligodendrocytic myelin paranodal and inner loop protein | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | OMIM: 617200; MGI: 2657025; HomoloGene: 13237; GeneCards: OPALIN; OMA: OPALIN - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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| Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Opalin is a protein that is encoded in humans by the OPALIN gene. [4] [5] [6]
References
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000050121 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ Nobile C, Hinzmann B, Scannapieco P, Siebert R, Zimbello R, Perez-Tur J, et al. (Jan 2002). "Identification and characterization of a novel human brain-specific gene, homologous to S. scrofa tmp83.5, in the chromosome 10q24 critical region for temporal lobe epilepsy and spastic paraplegia". Gene. 282 (1–2): 87–94. doi: 10.1016/S0378-1119(01)00846-0. PMID 11814680.
- ^ Aruga J, Yoshikawa F, Nozaki Y, Sakaki Y, Toyoda A, Furuichi T (Sep 2007). "An oligodendrocyte enhancer in a phylogenetically conserved intron region of the mammalian myelin gene Opalin". Journal of Neurochemistry. 102 (5): 1533–47. doi: 10.1111/j.1471-4159.2007.04583.x. PMID 17442045. S2CID 4231906.
- ^ "Entrez Gene: TMEM10 transmembrane protein 10".
Further reading
- Hartley JL, Temple GF, Brasch MA (Nov 2000). "DNA cloning using in vitro site-specific recombination". Genome Research. 10 (11): 1788–95. doi: 10.1101/gr.143000. PMC 310948. PMID 11076863.
- Simpson JC, Wellenreuther R, Poustka A, Pepperkok R, Wiemann S (Sep 2000). "Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing". EMBO Reports. 1 (3): 287–92. doi: 10.1093/embo-reports/kvd058. PMC 1083732. PMID 11256614.
- Wiemann S, Arlt D, Huber W, Wellenreuther R, Schleeger S, Mehrle A, Bechtel S, Sauermann M, Korf U, Pepperkok R, Sültmann H, Poustka A (Oct 2004). "From ORFeome to biology: a functional genomics pipeline". Genome Research. 14 (10B): 2136–44. doi: 10.1101/gr.2576704. PMC 528930. PMID 15489336.
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| This article on a gene on human chromosome 10 is a stub. You can help Wikipedia by expanding it. |