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 | 166 | 49 | 116 |
| Samples | 160 | 49 | 110 |
| Peptides | 99 | 24 | 82 |
Function
HLA-DOA · Major histocompatibility complex, class II, DO alpha
HLA-DOA belongs to the HLA class II alpha chain paralogues. HLA-DOA forms a heterodimer with HLA-DOB. The heterodimer, HLA-DO, is found in lysosomes in B cells and regulates HLA-DM-mediated peptide loading on MHC class II molecules. In comparison with classical HLA class II molecules, this gene exhibits very little sequence variation, especially at the protein level. [provided by RefSeq, Jul 2008].
Isoforms & Proteins
1 transcript · 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.
| Transcript | UniProt | Mutations | Peptides |
|---|---|---|---|
| ENST00000229829 | P06340 | 166 | 99 |
Gene Properties
Recurrent Mutations
All 99 amino-acid changes on canonical ENST00000229829 · 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 HLA-DOA · cell line vs tissue
For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in HLA-DOA – 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 |
|---|---|---|
| Unknown | 0/10 0% | 1/29 3% |
| T-Lymphoblastic Leukemia | 1/40 2% | 0/0 0% |
| Oral Cavity Carcinoma | 1/54 2% | 0/0 0% |
| Endometrial Carcinoma | 1/42 2% | 7/612 1% |
| Glioblastoma | 1/98 1% | 0/0 0% |
| Melanoma | 3/210 1% | 18/1899 1% |
| Hodgkins Lymphoma | 0/16 0% | 1/122 1% |
| Bladder Carcinoma | 3/58 5% | 4/956 0% |
| Neuroendocrine Tumour | 5/154 3% | 0/577 0% |
| Non-Small Cell Lung Carcinoma | 6/304 2% | 4/1390 0% |
| Colorectal Carcinoma | 3/143 2% | 15/3239 0% |
| Biliary Tract Carcinoma | 0/54 0% | 5/950 1% |
| Head and Neck Carcinoma | 3/85 4% | 4/1574 0% |
| Kidney Carcinoma | 3/85 4% | 5/1862 0% |
| Gastric Carcinoma | 2/74 3% | 4/1809 0% |
| Plasma Cell Myeloma | 0/44 0% | 1/305 0% |
| Neuroblastoma | 4/87 5% | 0/1331 0% |
| Ovarian Carcinoma | 0/109 0% | 3/998 0% |
| Hepatocellular Carcinoma | 2/46 4% | 4/2210 0% |
| Other Sarcomas | 0/69 0% | 2/699 0% |
| Other Solid Cancers | 0/94 0% | 4/1515 0% |
| Esophageal Carcinoma | 0/23 0% | 2/769 0% |
| Pancreatic Carcinoma | 2/89 2% | 2/1611 0% |
| Prostate Carcinoma | 0/13 0% | 5/2105 0% |
| Medulloblastoma | 0/0 0% | 1/450 0% |
| Breast Carcinoma | 3/144 2% | 3/3264 0% |
| Glioma | 0/52 0% | 4/2127 0% |
| Thyroid Gland Carcinoma | 0/45 0% | 3/1592 0% |
| Esophageal Squamous Cell Carcinoma | 2/51 4% | 2/2550 0% |
| Other Blood Cancers | 1/61 2% | 3/2725 0% |
Mutation Distribution
Where HLA-DOA is mutated · all tissues, split by cell line vs tissue
How many mutations in HLA-DOA 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 166 mutations in HLA-DOA
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 |
|---|