There is another report that miR-202 (probably miR-202-3p, since miR-202-5p was displayed as miR-202* in the earlier version of miRBase) is upregulated in the cerebellums of patients with MSA, in correlation with reductions in the expression of the organic cation uptake transporter (Oct1, encoded by SLC22A1) [117]. The gene discussed is SLC22A1; the disease is multiple system atrophy.