EMC10
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.
