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 | 385 | 82 | 297 |
| Samples | 350 | 70 | 277 |
| Peptides | 257 | 43 | 217 |
Function
PRKCI · Protein kinase C iota
This gene encodes a member of the protein kinase C (PKC) family of serine/threonine protein kinases. The PKC family comprises at least eight members, which are differentially expressed and are involved in a wide variety of cellular processes. This protein kinase is calcium-independent and phospholipid-dependent. It is not activated by phorbolesters or diacylglycerol. This kinase can be recruited to vesicle tubular clusters (VTCs) by direct interaction with the small GTPase RAB2, where this kinase phosphorylates glyceraldehyde-3-phosphate dehydrogenase (GAPD/GAPDH) and plays a role in microtubule dynamics in the early secretory pathway. This kinase is found to be necessary for BCL-ABL-mediated resistance to drug-induced apoptosis and therefore protects leukemia cells against drug-induced apoptosis. There is a single exon pseudogene mapped on chromosome X. [provided by RefSeq, Jul 2008].
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 |
|---|---|---|---|
| ENST00000295797 | P41743 | 385 | 257 |
Gene Properties
Recurrent Mutations
All 257 amino-acid changes on canonical ENST00000295797 · 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 PRKCI · cell line vs tissue
For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in PRKCI – 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% |
| Endometrial Carcinoma | 6/42 14% | 14/612 2% |
| Acute Myeloid Leukemia | 2/90 2% | 0/0 0% |
| Glioblastoma | 2/98 2% | 0/0 0% |
| Cervical Carcinoma | 0/35 0% | 9/422 2% |
| Melanoma | 8/210 4% | 31/1899 2% |
| Colorectal Carcinoma | 13/143 9% | 36/3239 1% |
| Squamous Cell Lung Carcinoma | 1/57 2% | 11/810 1% |
| Non-Small Cell Lung Carcinoma | 5/304 2% | 18/1390 1% |
| Other Solid Cancers | 2/94 2% | 18/1515 1% |
| Bladder Carcinoma | 2/58 3% | 10/956 1% |
| Gastric Carcinoma | 0/74 0% | 20/1809 1% |
| Thyroid Gland Carcinoma | 0/45 0% | 16/1592 1% |
| Ovarian Carcinoma | 3/109 3% | 7/998 1% |
| Head and Neck Carcinoma | 1/85 1% | 13/1574 1% |
| Gastrointestinal Stromal Tumour | 0/0 0% | 1/133 1% |
| Neuroendocrine Tumour | 2/154 1% | 3/577 1% |
| Small Cell Lung Carcinoma | 2/9 22% | 3/752 0% |
| Other Sarcomas | 2/69 3% | 3/699 0% |
| Biliary Tract Carcinoma | 0/54 0% | 6/950 1% |
| Plasma Cell Myeloma | 1/44 2% | 1/305 0% |
| Esophageal Squamous Cell Carcinoma | 2/51 4% | 12/2550 0% |
| Rhabdomyosarcoma | 1/33 3% | 0/171 0% |
| Burkitts Lymphoma | 1/32 3% | 0/196 0% |
| Breast Carcinoma | 0/144 0% | 15/3264 0% |
| Pancreatic Carcinoma | 3/89 3% | 4/1611 0% |
| Meningioma | 1/3 33% | 0/252 0% |
| Kidney Carcinoma | 3/85 4% | 4/1862 0% |
| Non-Cancerous | 0/104 0% | 3/830 0% |
| Hepatocellular Carcinoma | 0/46 0% | 7/2210 0% |
Mutation Distribution
Where PRKCI is mutated · all tissues, split by cell line vs tissue
How many mutations in PRKCI 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 385 mutations in PRKCI
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 |
|---|