RBM10 Polyclonal Antibody

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.

DXS8237E, G patch domain containing protein 9, G patch domain-containing protein 9, GPATC9, GPATCH9, HGNC9896, KIAA0122, MGC1132, MGC997, Rbm10, RBM10, RNA binding motif protein 10 , RNA binding protein 10, RNA binding protein S1-1, RNA-binding motif protein 10, RNA-b