ATP7B

ATPase copper transporting beta P35670 ATP7B_HUMAN
Protein Coding Chr 13 13q14.3 Swiss-Prot reviewed Entrez 540
Mutations
3,842
CL 511 · Tissue 3,220
Samples
733
CL 159 · Tissue 553
Peptides
673
unique mutant peptides
Transcripts
6
isoforms mutated

Stats by Source

Total, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)

How the counts split by source
Stats by Source

Total = all mutations for this gene across every source.

Cell line = COSMIC Cell Lines Project + DepMap + PubMed.

Tissue = COSMIC primary-tissue (patient tumour) samples.

Total can exceed cell line + tissue: COSMIC tissue-derived models sit only in global, and a peptide can be shared across both.

TotalCell lineTissue
Mutations3,8425113,220
Samples733159553
Peptides673125560

Function

ATP7B · ATPase copper transporting beta

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].

Isoforms & Proteins

6 transcripts · UniProt mapping is sequence-verified (AA-safe)

About the isoform mapping
Isoforms & Proteins

Each Ensembl transcript (ENST) this gene is mutated on, with its matched UniProt accession.

The mapping is sequence-verified: the UniProt sequence is identical to the transcript translation, so amino-acid positions line up exactly. A * marks an unreviewed (TrEMBL) entry.

Counts are mutations and unique mutant peptides on each transcript.

TranscriptUniProtMutationsPeptides
ENST00000242839 P35670 853 582
ENST00000400366 P35670-3 716 510
ENST00000634844 B7ZLR4* 709 506
ENST00000418097 F5H748* 702 502
ENST00000400370 F5H562* 516 372
ENST00000448424 E7ET55* 346 247

Gene Properties

Type
Protein Coding
Chromosome
13
Cytoband
13q14.3
Entrez ID
Aliases
PWDWC1WDWND

Recurrent Mutations

All 582 amino-acid changes on canonical ENST00000242839 · needle height = samples · drag the mini-map to zoom

What this lollipop shows
Recurrent Mutations

A lollipop / needle plot – the standard way to show recurrent mutations along a protein (as used by cBioPortal and MutationMapper).

X-axis = amino-acid position in the protein.

Needle height & head size = how often that exact amino-acid change was observed (its recurrence). Tall/large heads are mutational hotspots.

The most recurrent changes are labelled; hover any needle for the change, position and counts.

Mutation frequency across cancer types

% of samples with a missense/complex mutation in ATP7B · cell line vs tissue

How this frequency is counted
Cancer-type mutation frequency

For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in ATP7B – counted as distinct samples (a sample counts once no matter how many mutations it has).

Split into cell line and tissue; each cell shows mutated / total and the percentage. Cohorts with <20 samples are omitted. Ordered by combined frequency.

Cancer typeCell linesTissue samples
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
T-Cell Non-Hodgkins Lymphoma
2/26 8%
0/0 0%
T-Lymphoblastic Leukemia
3/40 8%
0/0 0%
Acute Myeloid Leukemia
5/90 6%
0/0 0%
Endometrial Carcinoma
6/42 14%
29/612 5%
Melanoma
12/210 6%
94/1899 5%
Hodgkins Lymphoma
3/16 19%
3/122 2%
Gastrointestinal Stromal Tumour
0/0 0%
5/133 4%
Colorectal Carcinoma
25/143 17%
73/3239 2%
Non-Small Cell Lung Carcinoma
21/304 7%
25/1390 2%
Ewings Sarcoma
1/63 2%
7/262 3%
Small Cell Lung Carcinoma
2/9 22%
16/752 2%
Other Solid Cancers
7/94 7%
31/1515 2%
Bladder Carcinoma
0/58 0%
23/956 2%
Gastric Carcinoma
2/74 3%
39/1809 2%
Squamous Cell Lung Carcinoma
6/57 11%
11/810 1%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Hepatocellular Carcinoma
2/46 4%
29/2210 1%
Cervical Carcinoma
0/35 0%
6/422 1%
Neuroendocrine Tumour
8/154 5%
1/577 0%
Glioma
5/52 10%
21/2127 1%
Meningioma
1/3 33%
2/252 1%
Other Sarcomas
1/69 1%
8/699 1%
Esophageal Carcinoma
2/23 9%
7/769 1%
Germ Cell Tumour
0/25 0%
2/169 1%
Biliary Tract Carcinoma
2/54 4%
8/950 1%
Thyroid Gland Carcinoma
3/45 7%
13/1592 1%
Non-Cancerous
0/104 0%
9/830 1%
Osteosarcoma
2/45 4%
0/166 0%
Esophageal Squamous Cell Carcinoma
2/51 4%
22/2550 1%

Mutation Distribution

Where ATP7B is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ATP7B were found in each tissue, across the whole database.

Each bar is a tissue (cell-line and tissue names are merged to the standard tissue), split into cell line and tissue (patient tumour) contributions.

This shows the cancer-context where this gene is recurrently altered.

GTEx Expression

Median TPM across 54 healthy tissues

GTEx Portal ↗
About the expression data
GTEx Expression

Median gene expression (TPM) in normal, non-cancer human tissues from the GTEx project.

Useful for judging tumour specificity – a strong neoantigen target ideally comes from a gene with low expression in healthy tissues.

Scroll or drag the mini-axis below the chart to browse all tissues.

Mutations

All 3,842 mutations in ATP7B

About the mutation list
Mutations

Every mutation record for this gene, across all samples and sources.

The Sample column links to the cell line (cell-line samples) or the tissue type (tissue samples).

Use the Type / Source filters, the search box, and column sorting to explore; each CAN-IMMUNE ID opens the full mutation & peptide view.

IDSampleTranscriptAA Change CDSTypeSourceMutant PeptideWild-type Peptide