MEG8
In molecular biology, Maternally expressed 8 (non-protein coding), also known as MEG8 or Rian (RNA Imprinted and Accumulated in Nucleus), is a long non-coding RNA. It is an imprinted gene, which is maternally expressed. It is expressed in the nucleus and (in an eight-week-old sheep) is preferentially expressed in skeletal muscle.[2][3]
| MEG8 | |||||||||||||||||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Aliases | MEG8, maternally expressed 8 (non-protein coding), Bsr, Irm, LINC00024, NCRNA00024, Rian, maternally expressed 8, small nucleolar RNA host gene, SNHG23, SNHG24, lnc-MGC | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | OMIM: 613648 GeneCards: MEG8 | ||||||||||||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||||||||||||
| Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||||||||||||
See also
References
- "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- Hatada I, Morita S, Obata Y, Sotomaru Y, Shimoda M, Kono T (August 2001). "Identification of a new imprinted gene, Rian, on mouse chromosome 12 by fluorescent differential display screening". Journal of Biochemistry. 130 (2): 187–90. doi:10.1093/oxfordjournals.jbchem.a002971. PMID 11481034.
- Charlier C, Segers K, Wagenaar D, Karim L, Berghmans S, Jaillon O, et al. (May 2001). "Human-ovine comparative sequencing of a 250-kb imprinted domain encompassing the callipyge (clpg) locus and identification of six imprinted transcripts: DLK1, DAT, GTL2, PEG11, antiPEG11, and MEG8". Genome Research. 11 (5): 850–62. doi:10.1101/gr.172701. PMC 311092. PMID 11337479.
Further reading
- Cavaillé J, Seitz H, Paulsen M, Ferguson-Smith AC, Bachellerie JP (June 2002). "Identification of tandemly-repeated C/D snoRNA genes at the imprinted human 14q32 domain reminiscent of those at the Prader-Willi/Angelman syndrome region". Human Molecular Genetics. 11 (13): 1527–38. doi:10.1093/hmg/11.13.1527. PMID 12045206.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.