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 | 451 | 63 | 380 |
| Samples | 221 | 44 | 172 |
| Peptides | 173 | 26 | 150 |
Function
ZFP36L1 · ZFP36 like 1 zinc finger CCCH-type
This gene is a member of the TIS11 family of early response genes, which are induced by various agonists such as the phorbol ester TPA and the polypeptide mitogen EGF. This gene is well conserved across species and has a promoter that contains motifs seen in other early-response genes. The encoded protein contains a distinguishing putative zinc finger domain with a repeating cys-his motif. This putative nuclear transcription factor most likely functions in regulating the response to growth factors. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011].
Isoforms & Proteins
3 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 172 amino-acid changes on canonical ENST00000439696 · 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 ZFP36L1 · cell line vs tissue
For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in ZFP36L1 – 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 |
|---|---|---|
| Hodgkins Lymphoma | 0/16 0% | 8/122 7% |
| T-Lymphoblastic Leukemia | 2/40 5% | 0/0 0% |
| Burkitts Lymphoma | 2/32 6% | 4/196 2% |
| Thymic Epithelial Tumor | 0/0 0% | 1/39 3% |
| Bladder Carcinoma | 1/58 2% | 17/956 2% |
| Endometrial Carcinoma | 3/42 7% | 5/612 1% |
| Acute Myeloid Leukemia | 1/90 1% | 0/0 0% |
| B-Cell Non-Hodgkins Lymphoma | 9/88 10% | 17/2534 1% |
| Non-Small Cell Lung Carcinoma | 4/304 1% | 11/1390 1% |
| Plasma Cell Myeloma | 1/44 2% | 2/305 1% |
| Neuroendocrine Tumour | 3/154 2% | 3/577 1% |
| Squamous Cell Lung Carcinoma | 0/57 0% | 7/810 1% |
| Melanoma | 2/210 1% | 14/1899 1% |
| Cervical Carcinoma | 0/35 0% | 3/422 1% |
| Other Solid Cancers | 0/94 0% | 10/1515 1% |
| Colorectal Carcinoma | 2/143 1% | 17/3239 1% |
| Germ Cell Tumour | 0/25 0% | 1/169 1% |
| Other Sarcomas | 2/69 3% | 2/699 0% |
| Medulloblastoma | 0/0 0% | 2/450 0% |
| Biliary Tract Carcinoma | 1/54 2% | 3/950 0% |
| Small Cell Lung Carcinoma | 1/9 11% | 2/752 0% |
| Esophageal Squamous Cell Carcinoma | 0/51 0% | 9/2550 0% |
| Prostate Carcinoma | 1/13 8% | 6/2105 0% |
| Head and Neck Carcinoma | 0/85 0% | 5/1574 0% |
| Gastric Carcinoma | 2/74 3% | 3/1809 0% |
| Hepatocellular Carcinoma | 0/46 0% | 6/2210 0% |
| Other Blood Cancers | 2/61 3% | 4/2725 0% |
| Non-Cancerous | 1/104 1% | 1/830 0% |
| Breast Carcinoma | 0/144 0% | 6/3264 0% |
| Ovarian Carcinoma | 1/109 1% | 1/998 0% |
Mutation Distribution
Where ZFP36L1 is mutated · all tissues, split by cell line vs tissue
How many mutations in ZFP36L1 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 451 mutations in ZFP36L1
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 |
|---|