USP9X Rabbit mAb

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. Synonyma: FAF, FAM, hFAM, DFFRX, MRX99, XLID99, MRXS99F, USP9X