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Gene Expression Literature Summary
Symbol
Name
ID
Nipa1
non imprinted in Prader-Willi/Angelman syndrome 1 homolog (human)
MGI:2442058

1 matching records from 1 references.

Summary by Age and Assay: Numbers in the table indicate the number of results matching the search criteria.
Age E12.5 E14.5 E16.5 E18.5 P
In situ RNA (section) 1 1 1 1 1

Summary by Gene and Reference: Number indicates the number of results matching the search criteria recorded for each reference.
* Indicates detailed expression data entries available
Nipa1  non imprinted in Prader-Willi/Angelman syndrome 1 homolog (human)   (Synonyms: 1110027G09Rik, A830014A18Rik, Spg6)
Results  Reference
5*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

Contributing Projects:
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
04/16/2024
MGI 6.23
The Jackson Laboratory