Rabbit Anti-Human ANKRD11 polyclonal antibody for ELISA, IHC (PFA fixed), WB. This locus encodes an ankryin repeat domain-containing protein. The encoded protein inhibits ligand-dependent;activation of transcription. Mutations in this gene have been associated with KBG syndrome, which is characterized by;macrodontia, distinctive craniofacial features, short stature, skeletal anomalies, global developmental delay,;seizures and intellectual disability. Alternatively spliced transcript variants have been described. Related;pseudogenes exist on chromosomes 2 and X.