In the HD model, SLC25A8 (UCP2) and SLC25A48 were downregulated (2–3 fold) and significant (about 2 fold) upregulation was observed in the HD model for SLCA13 (aspartate/glutamate carrier 2) and for SLC25A32 (mitochondrial folate transporter). This evidence concerns the gene SLC25A32 and Huntington disease.