TMEM126A Back

transmembrane protein 126A

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NCBI Description of TMEM126A
The protein encoded by this gene is a mitochondrial membrane protein of unknown function. Defects in this gene are a cause of optic atrophy type 7 (OPA7). Two transcript variants encoding different isoforms have been found for this gene.

Community Annotation of TMEM126A Add / Edit TMEM126A: Annotations

No community annotations yet for TMEM126A.
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Figure notes


• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


Legend

TMEM126A is highly significantly mutated in
(none)
TMEM126A is significantly mutated in
(none)
TMEM126A is near significance in
(none)

Click on a tumor type to see its full list of significant genes.

Data details


• Mutation list for TMEM126A