Assay
Age
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In situ RNA (section)
15.5 DPC
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Ndn necdin, MAGE family member (Synonyms: Peg6) | |
Results | Reference |
1 | 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 |
1 | J:82266 Ren J, Lee S, Pagliardini S, Gerard M, Stewart CL, Greer JJ, Wevrick R, Absence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal mice. J Neurosci. 2003 Mar 1;23(5):1569-73 |
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 05/14/2024 MGI 6.23 |
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