Symbol Name ID |
Gfap
glial fibrillary acidic protein MGI:95697 |
Reference
|
J:183239 Shekarabi M, Moldrich RX, Rasheed S, Salin-Cantegrel A, Laganiere J, Rochefort D, Hince P, Huot K, Gaudet R, Kurniawan N, Sotocinal SG, Ritchie J, Dion PA, Mogil JS, Richards LJ, Rouleau GA, Loss of neuronal potassium/chloride cotransporter 3 (KCC3) is responsible for the degenerative phenotype in a conditional mouse model of hereditary motor and sensory neuropathy associated with agenesis of the corpus callosum. J Neurosci. 2012 Mar 14;32(11):3865-76 |
Age | E17.5 |
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 11/19/2024 MGI 6.24 |
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