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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