Lentiviral human ATP7B sgRNA gene knockout kit

Human ATP7B

Gene symbol: ATP7B
Synonyms: PWD WC1 WD WND
Species: HUMAN
Gene ID: 540
Summary: This gene is a member of the P-type cation transport ATPase family and encodes a protein with several membrane-spanning domains, an ATPase consensus sequence, a hinge domain, a phosphorylation site, and at least 2 putative copper-binding sites. This protein functions as a monomer, exporting copper out of the cells, such as the efflux of hepatic copper into the bile. Alternate transcriptional splice variants, encoding different isoforms with distinct cellular localizations, have been characterized. Mutations in this gene have been associated with Wilson disease (WD). [provided by RefSeq, Jul 2008].
NM numbers targeted (Accession number:Exon:CDS Fragment): NM_000053:4:4 NM_001330578:4:4 NM_001330579:4:4 NM_001243182:5:5 NM_001005918:4:4