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 | 46 | 39 | 0 |
| Samples | 43 | 36 | 0 |
| Peptides | 44 | 37 | 0 |
Function
ODAD3 · Outer dynein arm docking complex subunit 3
This gene encodes a protein containing coiled-coil domains. The encoded protein functions in outer dynein arm assembly and is required for motile cilia function. Mutations in this gene result in primary ciliary dyskinesia. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2014].
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 |
|---|---|---|---|
| ENST00000356392 | A5D8V7 | 46 | 44 |
Gene Properties
Recurrent Mutations
All 44 amino-acid changes on canonical ENST00000356392 · 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 ODAD3 · cell line vs tissue
For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in ODAD3 – 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 | 3/40 8% | 0/0 0% |
| T-Cell Non-Hodgkins Lymphoma | 1/26 4% | 0/0 0% |
| Oral Cavity Carcinoma | 2/54 4% | 0/0 0% |
| Glioblastoma | 3/98 3% | 0/0 0% |
| Burkitts Lymphoma | 2/32 6% | 0/196 0% |
| Rhabdomyosarcoma | 1/33 3% | 0/171 0% |
| Endometrial Carcinoma | 3/42 7% | 0/612 0% |
| Squamous Cell Lung Carcinoma | 3/57 5% | 0/810 0% |
| Plasma Cell Myeloma | 1/44 2% | 0/305 0% |
| Non-Small Cell Lung Carcinoma | 3/304 1% | 1/1390 0% |
| Colorectal Carcinoma | 4/143 3% | 1/3239 0% |
| Neuroendocrine Tumour | 1/154 1% | 0/577 0% |
| Gastric Carcinoma | 0/74 0% | 2/1809 0% |
| Kidney Carcinoma | 1/85 1% | 1/1862 0% |
| Bladder Carcinoma | 1/58 2% | 0/956 0% |
| Biliary Tract Carcinoma | 0/54 0% | 1/950 0% |
| Ovarian Carcinoma | 1/109 1% | 0/998 0% |
| Glioma | 1/52 2% | 1/2127 0% |
| Head and Neck Carcinoma | 1/85 1% | 0/1574 0% |
| Melanoma | 1/210 0% | 0/1899 0% |
| Prostate Carcinoma | 1/13 8% | 0/2105 0% |
| Esophageal Squamous Cell Carcinoma | 1/51 2% | 0/2550 0% |
| Breast Carcinoma | 1/144 1% | 0/3264 0% |
Mutation Distribution
Where ODAD3 is mutated · all tissues, split by cell line vs tissue
How many mutations in ODAD3 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.
Mutations
All 46 mutations in ODAD3
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 |
|---|