NCBI Description of RBM10
|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.|
Community Annotation of RBM10 Add / Edit RBM10: Annotations
No community annotations yet for RBM10.
• "Mouse over" a mutation to see details.
Click on a tumor type to see its full list of significant genes.