Symbol Name ID |
Opa3
optic atrophy 3 MGI:2686271 |
Age | E8 | E10 | E10.5 | E11.5 | E12.5 | E13 | E14.5 | E15 | E16.5 | E17 | E18.5 | P |
Immunohistochemistry (section) | 1 | 1 | 2 | |||||||||
In situ RNA (section) | 1 | 1 | 1 | 1 | ||||||||
Western blot | 1 | 1 | ||||||||||
RT-PCR | 1 | 1 | 1 | 1 | 1 | 1 |
Opa3 optic atrophy 3 (Synonyms: D630048P19Rik, LOC243868, LOC384570) | |
Results | Reference |
5* | 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 |
11* | J:181412 Powell KA, Davies JR, Taylor E, Wride MA, Votruba M, Mitochondrial localization and ocular expression of mutant Opa3 in a mouse model of 3-methylglutaconicaciduria type III. Invest Ophthalmol Vis Sci. 2011 Jun;52(7):4369-80 |
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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