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 | 360 | 71 | 258 |
| Samples | 187 | 54 | 128 |
| Peptides | 170 | 46 | 122 |
Function
FSCN2 · Fascin actin-bundling protein 2, retinal
This gene encodes a member of the fascin protein family. Fascins crosslink actin into filamentous bundles within dynamic cell extensions. This family member is proposed to play a role in photoreceptor disk morphogenesis. A mutation in this gene results in one form of autosomal dominant retinitis pigmentosa and macular degeneration. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008].
Isoforms & Proteins
2 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 154 amino-acid changes on canonical ENST00000417245 · 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 FSCN2 · cell line vs tissue
For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in FSCN2 – 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 | 7/40 18% | 0/0 0% |
| Oral Cavity Carcinoma | 1/54 2% | 0/0 0% |
| Germ Cell Tumour | 0/25 0% | 3/169 2% |
| Endometrial Carcinoma | 4/42 10% | 4/612 1% |
| Melanoma | 2/210 1% | 18/1899 1% |
| Bladder Carcinoma | 1/58 2% | 7/956 1% |
| Colorectal Carcinoma | 5/143 4% | 21/3239 1% |
| Gastrointestinal Stromal Tumour | 0/0 0% | 1/133 1% |
| Squamous Cell Lung Carcinoma | 1/57 2% | 4/810 0% |
| Plasma Cell Myeloma | 0/44 0% | 2/305 1% |
| Neuroendocrine Tumour | 4/154 3% | 0/577 0% |
| Ovarian Carcinoma | 6/109 6% | 0/998 0% |
| Non-Cancerous | 1/104 1% | 4/830 0% |
| Non-Small Cell Lung Carcinoma | 5/304 2% | 4/1390 0% |
| Mesothelioma | 1/62 2% | 0/165 0% |
| Gastric Carcinoma | 1/74 1% | 7/1809 0% |
| Meningioma | 1/3 33% | 0/252 0% |
| Other Solid Cancers | 2/94 2% | 4/1515 0% |
| Ewings Sarcoma | 0/63 0% | 1/262 0% |
| Hepatocellular Carcinoma | 1/46 2% | 6/2210 0% |
| Biliary Tract Carcinoma | 0/54 0% | 3/950 0% |
| Glioma | 0/52 0% | 6/2127 0% |
| B-Cell Non-Hodgkins Lymphoma | 1/88 1% | 6/2534 0% |
| Esophageal Squamous Cell Carcinoma | 1/51 2% | 6/2550 0% |
| Kidney Carcinoma | 2/85 2% | 3/1862 0% |
| Other Sarcomas | 1/69 1% | 1/699 0% |
| Esophageal Carcinoma | 0/23 0% | 2/769 0% |
| Cervical Carcinoma | 0/35 0% | 1/422 0% |
| Prostate Carcinoma | 0/13 0% | 4/2105 0% |
| B-Lymphoblastic Leukemia | 1/55 2% | 4/2640 0% |
Mutation Distribution
Where FSCN2 is mutated · all tissues, split by cell line vs tissue
How many mutations in FSCN2 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 360 mutations in FSCN2
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 |
|---|