Symbol Name ID |
Snord116
small nucleolar RNA, C/D box 116 cluster MGI:1891407 |
Age | E7 | E7.5 | E9.5 | E10.5 | E11 | E12.5 | E13 | E13.5 | E15 | E15.5 | E17 | E18.5 | E | P |
In situ RNA (section) | 1 | 1 | 1 | 1 | 1 | 1 | ||||||||
In situ RNA (whole mount) | 1 | 1 | ||||||||||||
Northern blot | 1 | 2 | 1 | 2 | 1 | 1 | 3 | |||||||
RT-PCR | 1 | 2 | 1 | 4 |
Snord116 small nucleolar RNA, C/D box 116 cluster (Synonyms: MBII-85, Pwcr1) | |
Results | Reference |
4 | J:93285 Cavaille J, Seitz H, Paulsen M, Ferguson-Smith AC, Bachellerie JP, Identification of tandemly-repeated C/D snoRNA genes at the imprinted human 14q32 domain reminiscent of those at the Prader-Willi/Angelman syndrome region. Hum Mol Genet. 2002 Jul 15;11(13):1527-38 |
6* | J:65556 de Los Santos T, Schweizer J, Rees CA, Francke U, Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the prader-willi deletion region, which Is highly expressed in brain. Am J Hum Genet. 2000 Nov;67(5):1067-82 |
6 | J:85656 Lee S, Walker CL, Wevrick R, Prader-Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain. Gene Expr Patterns. 2003 Oct;3(5):599-609 |
4 | J:217174 Nakagaki A, Osanai H, Kishino T, Imprinting analysis of the mouse chromosome 7C region in DNMT1-null embryos. Gene. 2014 Dec 10;553(1):63-8 |
1 | J:112969 Ogawa H, Wu Q, Komiyama J, Obata Y, Kono T, Disruption of parental-specific expression of imprinted genes in uniparental fetuses. FEBS Lett. 2006 Oct 2;580(22):5377-84 |
1* | J:152022 Skryabin BV, Gubar LV, Seeger B, Pfeiffer J, Handel S, Robeck T, Karpova E, Rozhdestvensky TS, Brosius J, Deletion of the MBII-85 snoRNA gene cluster in mice results in postnatal growth retardation. PLoS Genet. 2007 Dec 28;3(12):e235 |
1 | J:172308 Stefan M, Simmons RA, Bertera S, Trucco M, Esni F, Drain P, Nicholls RD, Global deficits in development, function, and gene expression in the endocrine pancreas in a deletion mouse model of Prader-Willi syndrome. Am J Physiol Endocrinol Metab. 2011 May;300(5):E909-22 |
1 | J:101829 Watrin F, Le Meur E, Roeckel N, Ripoche MA, Dandolo L, Muscatelli F, The Prader-Willi syndrome murine imprinting center is not involved in the spatio-temporal transcriptional regulation of the Necdin gene. BMC Genet. 2005 Jan 5;6(1):1 |
3 | J:320211 Zhang Q, Bouma GJ, McClellan K, Tobet S, Hypothalamic expression of snoRNA Snord116 is consistent with a link to the hyperphagia and obesity symptoms of Prader-Willi syndrome. Int J Dev Neurosci. 2012 Oct;30(6):479-85 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 10/09/2024 MGI 6.24 |
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