Gene Expression Literature Detail
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Symbol Name ID |
Fam161a
family with sequence similarity 161, member A MGI:1921123 |
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Reference
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J:169188 Bandah-Rozenfeld D, Mizrahi-Meissonnier L, Farhy C, Obolensky A, Chowers I, Pe'er J, Merin S, Ben-Yosef T, Ashery-Padan R, Banin E, Sharon D, Homozygosity mapping reveals null mutations in FAM161A as a cause of autosomal-recessive retinitis pigmentosa. Am J Hum Genet. 2010 Sep 10;87(3):382-91 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | E12.5 | E14.5 | E16.5 | 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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