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 | 2,396 | 302 | 2,054 |
| Samples | 238 | 53 | 180 |
| Peptides | 200 | 32 | 176 |
Function
MBNL1 · Muscleblind like splicing regulator 1
This gene encodes a member of the muscleblind protein family which was initially described in Drosophila melanogaster. The encoded protein is a C3H-type zinc finger protein that modulates alternative splicing of pre-mRNAs. Muscleblind proteins bind specifically to expanded dsCUG RNA but not to normal size CUG repeats and may thereby play a role in the pathophysiology of myotonic dystrophy. Mice lacking this gene exhibited muscle abnormalities and cataracts. Several alternatively spliced transcript variants have been described but the full-length natures of only some have been determined. The different isoforms are thought to have different binding specificities and/or splicing activities. [provided by RefSeq, Sep 2015].
Isoforms & Proteins
14 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.
| Transcript | UniProt | Mutations | Peptides |
|---|---|---|---|
| ENST00000324210 | Q9NR56-5 | 212 | 131 |
| ENST00000282488 | A0A0A0MQX8* | 201 | 134 |
| ENST00000282486 | Q9NR56 | 195 | 129 |
| ENST00000463374 | Q9NR56 | 195 | 129 |
| ENST00000355460 | Q9NR56-2 | 175 | 119 |
| ENST00000498502 | C9JP00* | 175 | 116 |
| ENST00000493459 | Q86VM6* | 171 | 112 |
| ENST00000357472 | Q9NR56-6 | 160 | 110 |
| ENST00000492948 | Q9NR56-6 | 160 | 110 |
| ENST00000324196 | Q9NR56-7 | 157 | 110 |
| ENST00000485509 | Q9NR56-7 | 157 | 110 |
| ENST00000465907 | Q9NR56-4 | 148 | 98 |
| ENST00000545754 | Q9NR56-4 | 148 | 98 |
| ENST00000485910 | Q9NR56-3 | 142 | 93 |
Gene Properties
Recurrent Mutations
All 131 amino-acid changes on canonical ENST00000324210 · 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 MBNL1 · cell line vs tissue
For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in MBNL1 – 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 | 10/40 25% | 0/0 0% |
| Chronic Myelogenous Leukemia | 1/25 4% | 0/0 0% |
| Endometrial Carcinoma | 6/42 14% | 17/612 3% |
| Colorectal Carcinoma | 9/143 6% | 36/3239 1% |
| Melanoma | 7/210 3% | 19/1899 1% |
| Gastric Carcinoma | 0/74 0% | 19/1809 1% |
| Other Solid Cancers | 2/94 2% | 14/1515 1% |
| Neuroendocrine Tumour | 0/154 0% | 5/577 1% |
| Cervical Carcinoma | 0/35 0% | 3/422 1% |
| Small Cell Lung Carcinoma | 0/9 0% | 5/752 1% |
| Non-Small Cell Lung Carcinoma | 5/304 2% | 5/1390 0% |
| Squamous Cell Lung Carcinoma | 0/57 0% | 5/810 1% |
| Germ Cell Tumour | 0/25 0% | 1/169 1% |
| Glioma | 2/52 4% | 9/2127 0% |
| Biliary Tract Carcinoma | 0/54 0% | 5/950 1% |
| Hepatocellular Carcinoma | 1/46 2% | 10/2210 0% |
| Burkitts Lymphoma | 1/32 3% | 0/196 0% |
| Bladder Carcinoma | 2/58 3% | 2/956 0% |
| Esophageal Squamous Cell Carcinoma | 1/51 2% | 7/2550 0% |
| Other Sarcomas | 1/69 1% | 1/699 0% |
| Head and Neck Carcinoma | 2/85 2% | 2/1574 0% |
| Ovarian Carcinoma | 0/109 0% | 2/998 0% |
| Pancreatic Carcinoma | 2/89 2% | 1/1611 0% |
| Kidney Carcinoma | 1/85 1% | 2/1862 0% |
| Breast Carcinoma | 0/144 0% | 4/3264 0% |
| Other Blood Cancers | 0/61 0% | 3/2725 0% |
| B-Cell Non-Hodgkins Lymphoma | 0/88 0% | 3/2534 0% |
| B-Lymphoblastic Leukemia | 0/55 0% | 3/2640 0% |
| Thyroid Gland Carcinoma | 0/45 0% | 1/1592 0% |
| Prostate Carcinoma | 0/13 0% | 1/2105 0% |
Mutation Distribution
Where MBNL1 is mutated · all tissues, split by cell line vs tissue
How many mutations in MBNL1 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 2,396 mutations in MBNL1
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 |
|---|