{"symbol":"RBM10","synonyms":["S1-1","GPATCH9","TARPS","ZRANB5","DXS8237E","GPATC9"],"name":"RNA binding motif protein 10","description":"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.[provided by RefSeq, Mar 2011]","ncbiEntrezGeneId":8241,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/8241","proteins":[{"symbol":"RBM10_HUMAN","href":"/api/1.0/protein/RBM10_HUMAN"}],"hgncRootFamilies":[{"name":"Zinc fingers","href":"/api/1.0/gene_family/Zinc+fingers"},{"name":"RNA binding motif containing (RBM)","href":"/api/1.0/gene_family/RNA+binding+motif+containing+%28RBM%29"},{"name":"G patch domain containing (GPATCH)","href":"/api/1.0/gene_family/G+patch+domain+containing+%28GPATCH%29"}]}