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 | 322 | 47 | 266 |
| Samples | 276 | 46 | 226 |
| Peptides | 124 | 26 | 101 |
Function
KRTAP5-5 · Keratin associated protein 5-5
Predicted to act upstream of or within hematopoietic progenitor cell differentiation. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Apr 2022]
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 |
|---|---|---|---|
| ENST00000399676 | Q701N2 | 322 | 124 |
Gene Properties
Recurrent Mutations
All 127 amino-acid changes on canonical ENST00000399676 · 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 KRTAP5-5 · cell line vs tissue
For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in KRTAP5-5 – 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% | 6/133 5% |
| Melanoma | 5/210 2% | 37/1899 2% |
| Non-Small Cell Lung Carcinoma | 7/304 2% | 17/1390 1% |
| Endometrial Carcinoma | 2/42 5% | 6/612 1% |
| Squamous Cell Lung Carcinoma | 1/57 2% | 9/810 1% |
| Plasma Cell Myeloma | 2/44 5% | 2/305 1% |
| Acute Myeloid Leukemia | 1/90 1% | 0/0 0% |
| Glioblastoma | 1/98 1% | 0/0 0% |
| Thyroid Gland Carcinoma | 0/45 0% | 16/1592 1% |
| Cervical Carcinoma | 1/35 3% | 3/422 1% |
| Burkitts Lymphoma | 2/32 6% | 0/196 0% |
| Small Cell Lung Carcinoma | 0/9 0% | 6/752 1% |
| Colorectal Carcinoma | 3/143 2% | 23/3239 1% |
| Hodgkins Lymphoma | 0/16 0% | 1/122 1% |
| Ovarian Carcinoma | 1/109 1% | 7/998 1% |
| Bladder Carcinoma | 0/58 0% | 7/956 1% |
| Gastric Carcinoma | 0/74 0% | 12/1809 1% |
| Other Solid Cancers | 2/94 2% | 8/1515 1% |
| Neuroendocrine Tumour | 2/154 1% | 2/577 0% |
| Other Blood Cancers | 0/61 0% | 14/2725 1% |
| Rhabdomyosarcoma | 1/33 3% | 0/171 0% |
| Osteosarcoma | 1/45 2% | 0/166 0% |
| B-Cell Non-Hodgkins Lymphoma | 0/88 0% | 11/2534 0% |
| Kidney Carcinoma | 1/85 1% | 7/1862 0% |
| Other Sarcomas | 1/69 1% | 2/699 0% |
| Prostate Carcinoma | 0/13 0% | 8/2105 0% |
| Glioma | 2/52 4% | 5/2127 0% |
| Biliary Tract Carcinoma | 0/54 0% | 3/950 0% |
| Esophageal Squamous Cell Carcinoma | 0/51 0% | 7/2550 0% |
| Breast Carcinoma | 5/144 3% | 4/3264 0% |
Mutation Distribution
Where KRTAP5-5 is mutated · all tissues, split by cell line vs tissue
How many mutations in KRTAP5-5 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 8 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 322 mutations in KRTAP5-5
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 |
|---|