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Symbol Name ID |
Prom1
prominin 1 MGI:1100886 |
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Reference
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J:59407 Maw MA, Corbeil D, Koch J, Hellwig A, Wilson-Wheeler JC, Bridges RJ, Kumaramanickavel G, John S, Nancarrow D, Roper K, Weigmann A, Huttner WB, Denton MJ, A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration. Hum Mol Genet. 2000 Jan 1;9(1):27-34 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | E10 | E12 | P |
| Immunohistochemistry (section) | ![]() |
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| In situ RNA (section) | |||
| Immunohistochemistry (whole mount) | |||
| In situ RNA (whole mount) | |||
| In situ reporter (knock in) | |||
| Northern blot | |||
| Western blot | ![]() |
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| 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 09/30/2025 MGI 6.24 |
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