ATP7B Chromosome 13

ATPase copper transporting beta
892 variants 892 Health Risk

Upload your DNA to see your personal genotypes for variants in ATP7B.

What This Gene Does
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 is a monomer, and functions as a copper-transporting ATPase which exports 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 which is characterized by copper accumulation. [provided by RefSeq, Dec 2019]
Gene Info
Gene Group
ATPase copper transporting
Locus Type
gene with protein product
Location
13q14.3
Ensembl
ENSG00000123191
Associated Conditions (29)
Wilson disease
Inborn genetic diseases
ATP7B-related disorder
See cases
Uterine corpus endometrial carcinoma
Ovarian serous cystadenocarcinoma
Thyroid cancer
nonmedullary
1
Acute myeloid leukemia
Hepatocellular carcinoma
Familial cancer of breast
Intellectual disability
Wolff type
Epileptic encephalopathy
Malignant tumor of urinary bladder
Neoplasm
Kayser-Fleischer ring
Hand tremor
Developmental and epileptic encephalopathy 93
+9 more conditions
Key Variants
All Variants (892)
RSID Category Clinical Significance Conditions
RS1412025509 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1412593296 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1444841250 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1469425216 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1486594906 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1555282191 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1555282316 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1555284021 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1555286522 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1555287300 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1555288385 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1555291147 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1555291195 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1555291801 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1555294398 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease, Wilson disease
RS1555296356 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1566441447 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1566462533 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1566603492 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1593671769 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1593681941 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1593726081 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1593787789 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS181388674 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease, Wilson disease
RS184388696 Health Risk Pathogenic/Likely pathogenic Wilson disease, Familial cancer of breast, Wilson disease
RS193922102 Health Risk Pathogenic/Likely pathogenic Wilson disease, ATP7B-related disorder, Wilson disease
RS193922107 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS193922110 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1951978776 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1951995448 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1952001328 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1952004098 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1954023351 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1956914257 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1957032734 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1957151127 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1957506216 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1957514480 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1957520924 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1957898187 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1958431105 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease, Wilson disease
RS1958493213 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1958499462 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS1958503241 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS199623434 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS201038679 Health Risk Pathogenic/Likely pathogenic Wilson disease, Inborn genetic diseases, Wilson disease
RS201738967 Health Risk Pathogenic/Likely pathogenic Wilson disease, Inborn genetic diseases, ATP7B-related disorder
RS2138407151 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS2138414735 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
RS2138560807 Health Risk Pathogenic/Likely pathogenic Wilson disease, Wilson disease
Sign Up to Analyze Your DNA Log In