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Gene Expression Literature Summary
Symbol
Name
ID
Opa3
optic atrophy 3
MGI:2686271

2 matching records from 2 references.

Summary by Age and Assay: Numbers in the table indicate the number of results matching the search criteria.
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

Summary by Gene and Reference: Number indicates the number of results matching the search criteria recorded for each reference.
* Indicates detailed expression data entries available
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

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
08/15/2017
MGI 6.10
The Jackson Laboratory