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 | 221 | 32 | 188 |
| Samples | 199 | 32 | 166 |
| Peptides | 132 | 21 | 117 |
Function
KRTAP10-5 · Keratin associated protein 10-5
This is an intronless gene located in a cluster of related genes on the q arm of chromosome 21. The proteins encoded by these genes form disulfide bonds with cysteine residues in hair keratins, thereby contributing to the structure and stability of hair fibers. [provided by RefSeq, Apr 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 |
|---|---|---|---|
| ENST00000400372 | P60370 | 221 | 132 |
Gene Properties
Recurrent Mutations
All 132 amino-acid changes on canonical ENST00000400372 · 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 KRTAP10-5 · cell line vs tissue
For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in KRTAP10-5 – 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 |
|---|---|---|
| Gastrointestinal Stromal Tumour | 0/0 0% | 4/133 3% |
| Glioblastoma | 2/98 2% | 0/0 0% |
| Melanoma | 1/210 0% | 32/1899 2% |
| Cervical Carcinoma | 0/35 0% | 6/422 1% |
| Endometrial Carcinoma | 0/42 0% | 8/612 1% |
| Chondrosarcoma | 0/14 0% | 1/75 1% |
| Non-Small Cell Lung Carcinoma | 6/304 2% | 10/1390 1% |
| Squamous Cell Lung Carcinoma | 0/57 0% | 8/810 1% |
| Adrenocortical Carcinoma | 1/3 33% | 0/112 0% |
| Thyroid Gland Carcinoma | 1/45 2% | 13/1592 1% |
| Plasma Cell Myeloma | 2/44 5% | 0/305 0% |
| Other Solid Cancers | 0/94 0% | 9/1515 1% |
| Neuroendocrine Tumour | 1/154 1% | 3/577 1% |
| Bladder Carcinoma | 0/58 0% | 5/956 1% |
| Head and Neck Carcinoma | 1/85 1% | 7/1574 0% |
| Osteosarcoma | 0/45 0% | 1/166 1% |
| Glioma | 1/52 2% | 9/2127 0% |
| Ovarian Carcinoma | 3/109 3% | 2/998 0% |
| Colorectal Carcinoma | 6/143 4% | 9/3239 0% |
| Breast Carcinoma | 5/144 3% | 7/3264 0% |
| Non-Cancerous | 0/104 0% | 3/830 0% |
| Gastric Carcinoma | 1/74 1% | 5/1809 0% |
| Hepatocellular Carcinoma | 0/46 0% | 7/2210 0% |
| Esophageal Carcinoma | 0/23 0% | 2/769 0% |
| Other Blood Cancers | 1/61 2% | 5/2725 0% |
| Biliary Tract Carcinoma | 0/54 0% | 2/950 0% |
| Other Sarcomas | 0/69 0% | 1/699 0% |
| B-Cell Non-Hodgkins Lymphoma | 0/88 0% | 3/2534 0% |
| Neuroblastoma | 0/87 0% | 1/1331 0% |
| Prostate Carcinoma | 0/13 0% | 1/2105 0% |
Mutation Distribution
Where KRTAP10-5 is mutated · all tissues, split by cell line vs tissue
How many mutations in KRTAP10-5 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 1 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 221 mutations in KRTAP10-5
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 |
|---|