Gene Expression Literature Detail
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Symbol Name ID |
Nipa1
non imprinted in Prader-Willi/Angelman syndrome 1 homolog (human) MGI:2442058 |
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Reference
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J:161575 van der Zwaag B, Staal WG, Hochstenbach R, Poot M, Spierenburg HA, de Jonge MV, Verbeek NE, van 't Slot R, van Es MA, Staal FJ, Freitag CM, Buizer-Voskamp JE, Nelen MR, van den Berg LH, van Amstel HK, van Engeland H, Burbach JP, A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder. Am J Med Genet B Neuropsychiatr Genet. 2010 Jun 5;153B(4):960-6 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | E12.5 | E14.5 | E16.5 | E18.5 | P |
| Immunohistochemistry (section) | |||||
| In situ RNA (section) | |
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| 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 12/10/2024 MGI 6.24 |
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