This gene encodes a nuclear protein that belongs to a family proteins that contain an RNA-binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X-linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript variants.,RBM10,DXS8237E,GPATC9,GPATCH9,S1-1,TARPS,ZRANB5,Epigenetics & Nuclear Signaling,RNA Binding,RBM10