Symbol Name ID |
Fancl
Fanconi anemia, complementation group L MGI:1914280 |
Reference
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J:193641 Nakano Y, Jahan I, Bonde G, Sun X, Hildebrand MS, Engelhardt JF, Smith RJ, Cornell RA, Fritzsch B, Banfi B, A mutation in the Srrm4 gene causes alternative splicing defects and deafness in the Bronx waltzer mouse. PLoS Genet. 2012;8(10):e1002966 |
Age | 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 10/29/2024 MGI 6.24 |
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