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 | 1,518 | 191 | 1,308 |
| Samples | 390 | 75 | 310 |
| Peptides | 321 | 54 | 270 |
Function
RNF111 · Ring finger protein 111
The protein encoded by this gene is a nuclear RING-domain containing E3 ubiquitin ligase. This protein interacts with the transforming growth factor (TGF) -beta/NODAL signaling pathway by promoting the ubiquitination and proteosomal degradation of negative regulators, like SMAD proteins, and thereby enhances TGF-beta target-gene transcription. As a modulator of the nodal signaling cascade, this gene plays a critical role in the induction of mesoderm during embryonic development. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2012].
Isoforms & Proteins
4 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 304 amino-acid changes on canonical ENST00000348370 · 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 RNF111 · cell line vs tissue
For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in RNF111 – 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 | 2/40 5% | 0/0 0% |
| Endometrial Carcinoma | 6/42 14% | 23/612 4% |
| Chronic Myelogenous Leukemia | 1/25 4% | 0/0 0% |
| Bladder Carcinoma | 3/58 5% | 21/956 2% |
| Melanoma | 3/210 1% | 37/1899 2% |
| Oral Cavity Carcinoma | 1/54 2% | 0/0 0% |
| Colorectal Carcinoma | 14/143 10% | 42/3239 1% |
| Gastrointestinal Stromal Tumour | 0/0 0% | 2/133 2% |
| Gastric Carcinoma | 0/74 0% | 25/1809 1% |
| Other Solid Cancers | 4/94 4% | 17/1515 1% |
| Non-Cancerous | 1/104 1% | 10/830 1% |
| Plasma Cell Myeloma | 3/44 7% | 1/305 0% |
| Non-Small Cell Lung Carcinoma | 7/304 2% | 12/1390 1% |
| Cervical Carcinoma | 1/35 3% | 4/422 1% |
| Neuroendocrine Tumour | 6/154 4% | 2/577 0% |
| Other Sarcomas | 3/69 4% | 5/699 1% |
| Squamous Cell Lung Carcinoma | 0/57 0% | 9/810 1% |
| Glioblastoma | 1/98 1% | 0/0 0% |
| Rhabdomyosarcoma | 2/33 6% | 0/171 0% |
| Biliary Tract Carcinoma | 0/54 0% | 9/950 1% |
| Small Cell Lung Carcinoma | 0/9 0% | 6/752 1% |
| Hepatocellular Carcinoma | 0/46 0% | 17/2210 1% |
| Ovarian Carcinoma | 2/109 2% | 6/998 1% |
| Ewings Sarcoma | 1/63 2% | 1/262 0% |
| Germ Cell Tumour | 0/25 0% | 1/169 1% |
| Esophageal Carcinoma | 2/23 9% | 2/769 0% |
| Esophageal Squamous Cell Carcinoma | 6/51 12% | 7/2550 0% |
| Glioma | 1/52 2% | 10/2127 0% |
| Mesothelioma | 0/62 0% | 1/165 1% |
| Burkitts Lymphoma | 1/32 3% | 0/196 0% |
Mutation Distribution
Where RNF111 is mutated · all tissues, split by cell line vs tissue
How many mutations in RNF111 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 1,518 mutations in RNF111
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 |
|---|