Symbol Name ID

Opa3 optic atrophy 3 MGI:2686271

Reference

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

Detailed expression data for these assays: 31 results

Indicates gene expression was analyzed but not necessarily detected.

Age	E10.5	E11.5	E14.5	E18.5	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