XPOT Rabbit Polyclonal Antibody, 100ul Vacuum Filter Mutations in this gene are

Mutations in this gene are associated with atypical hemolytic uremic syndrome and age-related macular degeneration in human patients

Abnormal coupling of beta-adrenergic receptor to G protein is involved in the pathogenesis of the failing heart

EWSR1 on chromosome 22

Mice lacking this gene exhibit early embryonic death

through binding and inhibition of the enzyme farnesyl diphospate synthase (FPPS)

XPOT Rabbit Polyclonal Antibody, 100ul Vacuum Filter Mutations in this gene areThis gene encodes a protein belonging to the RAN GTPase exportin family that mediates export of tRNA from the nucleus to the cytoplasm. Translocation of tRNA to the cytoplasm occurs once exportin has bound both tRNA and GTP bound RAN.