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 | 1,674 | 270 | 1,320 |
| Samples | 1,282 | 223 | 1,026 |
| Peptides | 1,121 | 162 | 951 |
Function
CHD6 · Chromodomain helicase DNA binding protein 6
This gene encodes a member of the SNF2/RAD54 helicase protein family. The encoded protein contains two chromodomains, a helicase domain, and an ATPase domain. Several multi-subunit protein complexes remodel chromatin to allow patterns of cell type-specific gene expression, and the encoded protein is thought to be a core member of one or more of these chromatin remodeling complexes. The encoded protein may function as a transcriptional repressor and is involved in the cellular repression of influenza virus replication. [provided by RefSeq, Jul 2013].
Isoforms & Proteins
2 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 1095 amino-acid changes on canonical ENST00000373233 · 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 CHD6 · cell line vs tissue
For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in CHD6 – 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 |
|---|---|---|
| T-Lymphoblastic Leukemia | 9/40 22% | 0/0 0% |
| Melanoma | 19/210 9% | 165/1899 9% |
| Endometrial Carcinoma | 5/42 12% | 49/612 8% |
| Oral Cavity Carcinoma | 4/54 7% | 0/0 0% |
| Hodgkins Lymphoma | 4/16 25% | 5/122 4% |
| Gastric Carcinoma | 13/74 18% | 96/1809 5% |
| Colorectal Carcinoma | 34/143 24% | 146/3239 5% |
| Cervical Carcinoma | 4/35 11% | 19/422 4% |
| Non-Small Cell Lung Carcinoma | 26/304 9% | 58/1390 4% |
| Bladder Carcinoma | 5/58 9% | 45/956 5% |
| Chondrosarcoma | 4/14 29% | 0/75 0% |
| Chronic Myelogenous Leukemia | 1/25 4% | 0/0 0% |
| Squamous Cell Lung Carcinoma | 9/57 16% | 21/810 3% |
| Acute Myeloid Leukemia | 3/90 3% | 0/0 0% |
| Other Solid Cancers | 0/94 0% | 49/1515 3% |
| Neuroendocrine Tumour | 3/154 2% | 17/577 3% |
| Unknown | 1/10 10% | 0/29 0% |
| Non-Cancerous | 3/104 3% | 19/830 2% |
| Ovarian Carcinoma | 5/109 5% | 20/998 2% |
| Biliary Tract Carcinoma | 3/54 6% | 18/950 2% |
| Hepatocellular Carcinoma | 3/46 7% | 44/2210 2% |
| Esophageal Carcinoma | 2/23 9% | 14/769 2% |
| Esophageal Squamous Cell Carcinoma | 3/51 6% | 46/2550 2% |
| Burkitts Lymphoma | 3/32 9% | 1/196 1% |
| Adrenocortical Carcinoma | 0/3 0% | 2/112 2% |
| Plasma Cell Myeloma | 1/44 2% | 5/305 2% |
| Small Cell Lung Carcinoma | 0/9 0% | 13/752 2% |
| Head and Neck Carcinoma | 2/85 2% | 26/1574 2% |
| Glioma | 4/52 8% | 31/2127 1% |
| Gastrointestinal Stromal Tumour | 0/0 0% | 2/133 2% |
Mutation Distribution
Where CHD6 is mutated · all tissues, split by cell line vs tissue
How many mutations in CHD6 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 1,674 mutations in CHD6
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 |
|---|