SLC25A29 is a gene that encodes a protein involved in the transport of molecules across the inner mitochondrial membrane. This protein is part of the solute carrier family, which plays a crucial role in cellular metabolism by facilitating the movement of various substrates necessary for energy production. Mutations in the SLC25A29 gene can lead to metabolic disorders, affecting how cells generate energy. Research on this gene helps scientists understand its functions and potential implications for diseases related to mitochondrial dysfunction, which can impact overall health and development.