Symbol Name ID |
Prom1
prominin 1 MGI:1100886 |
Reference
|
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 |
Age | E10 | E12 | 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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