Lentiviral human ANKRD11 sgRNA gene knockout kit

Human ANKRD11

Gene symbol: ANKRD11
Synonyms: ANCO-1 ANCO1 LZ16 T13
Species: HUMAN
Gene ID: 29123
Summary: 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. [provided by RefSeq, Jan 2012].
NM numbers targeted (Accession number:Exon:CDS Fragment): NM_001256182:10:7 NM_013275:9:7 NM_001256183:9:7