Name

ATP7B Gene

ATPase, Cu++ transporting, beta polypeptide

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]

ATP7BP1 Gene

ATPase, Cu++ transporting, beta polypeptide pseudogene 1

atp7b Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term atp7b in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

ATP7B Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for ATP7B from the Pathway Commons Protein-Protein Interactions dataset.

atp7binteracting Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term atp7binteracting in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.