Stats by Source
Total, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)
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.
| Total | Cell line | Tissue | |
|---|---|---|---|
| Mutations | 564 | 121 | 434 |
| Samples | 339 | 81 | 253 |
| Peptides | 290 | 54 | 238 |
Function
ATP6V0A2 · ATPase H+ transporting V0 subunit a2
The protein encoded by this gene is a subunit of the vacuolar ATPase (v-ATPase), an heteromultimeric enzyme that is present in intracellular vesicles and in the plasma membrane of specialized cells, and which is essential for the acidification of diverse cellular components. V-ATPase is comprised of a membrane peripheral V(1) domain for ATP hydrolysis, and an integral membrane V(0) domain for proton translocation. The subunit encoded by this gene is a component of the V(0) domain. Mutations in this gene are a cause of both cutis laxa type II and wrinkly skin syndrome. [provided by RefSeq, Jul 2009].
Isoforms & Proteins
3 transcripts · UniProt mapping is sequence-verified (AA-safe)
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.
Gene Properties
Recurrent Mutations
All 279 amino-acid changes on canonical ENST00000330342 · needle height = samples · drag the mini-map to zoom
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 ATP6V0A2 · cell line vs tissue
For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in ATP6V0A2 – 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 type | Cell lines | Tissue samples |
|---|---|---|
| Chordoma | 2/7 29% | 0/13 0% |
| Chronic Myelogenous Leukemia | 2/25 8% | 0/0 0% |
| T-Cell Non-Hodgkins Lymphoma | 1/26 4% | 0/0 0% |
| Acute Myeloid Leukemia | 3/90 3% | 0/0 0% |
| Endometrial Carcinoma | 8/42 19% | 13/612 2% |
| Thymic Epithelial Tumor | 0/0 0% | 1/39 3% |
| Rhabdomyosarcoma | 1/33 3% | 4/171 2% |
| Squamous Cell Lung Carcinoma | 0/57 0% | 18/810 2% |
| Ewings Sarcoma | 6/63 10% | 0/262 0% |
| Melanoma | 10/210 5% | 27/1899 1% |
| Gastrointestinal Stromal Tumour | 0/0 0% | 2/133 2% |
| Other Solid Cancers | 0/94 0% | 24/1515 2% |
| Colorectal Carcinoma | 16/143 11% | 34/3239 1% |
| Burkitts Lymphoma | 3/32 9% | 0/196 0% |
| Small Cell Lung Carcinoma | 2/9 22% | 6/752 1% |
| Gastric Carcinoma | 0/74 0% | 19/1809 1% |
| Bladder Carcinoma | 0/58 0% | 9/956 1% |
| Non-Small Cell Lung Carcinoma | 3/304 1% | 9/1390 1% |
| Neuroendocrine Tumour | 3/154 2% | 2/577 0% |
| Hepatocellular Carcinoma | 2/46 4% | 13/2210 1% |
| Biliary Tract Carcinoma | 0/54 0% | 6/950 1% |
| Prostate Carcinoma | 1/13 8% | 11/2105 1% |
| Germ Cell Tumour | 0/25 0% | 1/169 1% |
| Glioma | 2/52 4% | 9/2127 0% |
| Ovarian Carcinoma | 1/109 1% | 4/998 0% |
| Cervical Carcinoma | 0/35 0% | 2/422 0% |
| Mesothelioma | 0/62 0% | 1/165 1% |
| B-Cell Non-Hodgkins Lymphoma | 3/88 3% | 7/2534 0% |
| Head and Neck Carcinoma | 0/85 0% | 6/1574 0% |
| Esophageal Squamous Cell Carcinoma | 3/51 6% | 6/2550 0% |
Mutation Distribution
Where ATP6V0A2 is mutated · all tissues, split by cell line vs tissue
How many mutations in ATP6V0A2 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
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 564 mutations in ATP6V0A2
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.
| ID | Sample | Transcript | AA Change | CDS | Type | Source | Mutant Peptide | Wild-type Peptide |
|---|