EMC10

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Description

EMC10, also known as Mitochondrial Carrier 10 (SLC25A34), is a gene encoding a protein involved in the transport of molecules across the mitochondrial inner membrane. This protein plays a crucial role in maintaining mitochondrial function and cellular energy production. Mutations in the EMC10 gene have been linked to a variety of mitochondrial disorders, impacting various systems within the body.

Associated Diseases

• Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS)
• Leigh syndrome
• Myopathy
• Neurodegeneration
• Cardiomyopathy

Did you know?

EMC10 is expressed in various tissues, including the brain, heart, and skeletal muscle, highlighting its widespread role in cellular function.