Gene Expression Literature Detail
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Symbol Name ID |
Opa3
optic atrophy 3 MGI:2686271 |
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Reference
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J:236995 Navein AE, Cooke EJ, Davies JR, Smith TG, Wells LH, Ohazama A, Healy C, Sharpe PT, Evans SL, Evans BA, Votruba M, Wells T, Disrupted mitochondrial function in the Opa3L122P mouse model for Costeff Syndrome impairs skeletal integrity. Hum Mol Genet. 2016 Jun 15;25(12):2404-2416 |
Indicates gene expression was analyzed but not necessarily detected.
| Age | E10.5 | E11.5 | E14.5 | E18.5 | P |
| Immunohistochemistry (section) | |
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| 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 11/12/2024 MGI 6.24 |
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