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