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 | 1,259 | 256 | 978 |
| Samples | 1,003 | 207 | 781 |
| Peptides | 817 | 153 | 681 |
Function
MYH9 · Myosin heavy chain 9
This gene encodes a conventional non-muscle myosin; this protein should not be confused with the unconventional myosin-9a or 9b (MYO9A or MYO9B). The encoded protein is a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain which is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in this gene have been associated with non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness. [provided by RefSeq, Dec 2011].
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 810 amino-acid changes on canonical ENST00000216181 · 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 MYH9 · cell line vs tissue
For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in MYH9 – 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 | 13/40 32% | 0/0 0% |
| Chronic Myelogenous Leukemia | 4/25 16% | 0/0 0% |
| Endometrial Carcinoma | 12/42 29% | 32/612 5% |
| Gastric Carcinoma | 5/74 7% | 92/1809 5% |
| Colorectal Carcinoma | 32/143 22% | 108/3239 3% |
| Squamous Cell Lung Carcinoma | 6/57 11% | 27/810 3% |
| Cervical Carcinoma | 1/35 3% | 16/422 4% |
| Bladder Carcinoma | 0/58 0% | 37/956 4% |
| Melanoma | 9/210 4% | 65/1899 3% |
| Non-Small Cell Lung Carcinoma | 17/304 6% | 40/1390 3% |
| Other Solid Cancers | 5/94 5% | 42/1515 3% |
| Hodgkins Lymphoma | 2/16 12% | 2/122 2% |
| Neuroendocrine Tumour | 11/154 7% | 9/577 2% |
| Esophageal Squamous Cell Carcinoma | 10/51 20% | 59/2550 2% |
| Plasma Cell Myeloma | 5/44 11% | 4/305 1% |
| Unknown | 0/10 0% | 1/29 3% |
| Head and Neck Carcinoma | 2/85 2% | 38/1574 2% |
| Acute Myeloid Leukemia | 2/90 2% | 0/0 0% |
| Ovarian Carcinoma | 8/109 7% | 16/998 2% |
| Germ Cell Tumour | 1/25 4% | 3/169 2% |
| Other Sarcomas | 5/69 7% | 10/699 1% |
| Esophageal Carcinoma | 2/23 9% | 10/769 1% |
| Gastrointestinal Stromal Tumour | 0/0 0% | 2/133 2% |
| Non-Cancerous | 6/104 6% | 8/830 1% |
| Breast Carcinoma | 7/144 5% | 40/3264 1% |
| Burkitts Lymphoma | 2/32 6% | 1/196 1% |
| Biliary Tract Carcinoma | 1/54 2% | 12/950 1% |
| Thyroid Gland Carcinoma | 2/45 4% | 17/1592 1% |
| Chondrosarcoma | 0/14 0% | 1/75 1% |
| Kidney Carcinoma | 7/85 8% | 14/1862 1% |
Mutation Distribution
Where MYH9 is mutated · all tissues, split by cell line vs tissue
How many mutations in MYH9 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 1,259 mutations in MYH9
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 |
|---|