{"symbol":"USP9X","synonyms":["DFFRX","FAM","MRXS99F"],"name":"ubiquitin specific peptidase 9, X-linked","description":"This gene is a member of the peptidase C19 family and encodes a protein that is similar to ubiquitin-specific proteases. Though this gene is located on the X chromosome, it escapes X-inactivation. Mutations in this gene have been associated with Turner syndrome. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]","ncbiEntrezGeneId":8239,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/8239","proteins":[{"symbol":"USP9X_HUMAN","href":"/api/1.0/protein/USP9X_HUMAN"}],"hgncRootFamilies":[{"name":"X-linked mental retardation","href":"/api/1.0/gene_family/X-linked+mental+retardation"},{"name":"Ubiquitin-specific peptidases (USP)","href":"/api/1.0/gene_family/Ubiquitin-specific+peptidases+%28USP%29"}]}