Symbol Name ID |
Ndn
necdin, MAGE family member MGI:97290 |
Reference
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J:223046 Rieusset A, Schaller F, Unmehopa U, Matarazzo V, Watrin F, Linke M, Georges B, Bischof J, Dijkstra F, Bloemsma M, Corby S, Michel FJ, Wevrick R, Zechner U, Swaab D, Dudley K, Bezin L, Muscatelli F, Stochastic loss of silencing of the imprinted Ndn/NDN allele, in a mouse model and humans with prader-willi syndrome, has functional consequences. PLoS Genet. 2013;9(9):e1003752 |
Age | E10.5 | E12.5 | E14.5 | P |
Immunohistochemistry (section) | ||||
In situ RNA (section) | ||||
Immunohistochemistry (whole mount) | ||||
In situ RNA (whole mount) | ||||
In situ reporter (knock in) | ||||
Northern blot | ||||
Western blot | ||||
RT-PCR | ||||
cDNA clones | ||||
RNase protection | ||||
Nuclease S1 | ||||
Primer Extension |
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 11/12/2024 MGI 6.24 |
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