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 | 7,715 | 776 | 6,893 |
| Samples | 922 | 152 | 763 |
| Peptides | 818 | 141 | 727 |
Function
RUNX1T1 · RUNX1 partner transcriptional co-repressor 1
This gene encodes a member of the myeloid translocation gene family which interact with DNA-bound transcription factors and recruit a range of corepressors to facilitate transcriptional repression. The t(8;21)(q22;q22) translocation is one of the most frequent karyotypic abnormalities in acute myeloid leukemia. The translocation produces a chimeric gene made up of the 5'-region of the runt-related transcription factor 1 gene fused to the 3'-region of this gene. The chimeric protein is thought to associate with the nuclear corepressor/histone deacetylase complex to block hematopoietic differentiation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2010].
Isoforms & Proteins
9 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 |
|---|---|---|---|
| ENST00000520724 | Q06455-3 | 1,086 | 616 |
| ENST00000523629 | Q06455 | 985 | 551 |
| ENST00000396218 | Q06455-2 | 941 | 546 |
| ENST00000517919 | Q06455 | 907 | 533 |
| ENST00000436581 | A0A0A0MSU1* | 892 | 531 |
| ENST00000518844 | Q06455-2 | 874 | 514 |
| ENST00000360348 | Q06455-4 | 873 | 521 |
| ENST00000422361 | Q06455-4 | 848 | 503 |
| ENST00000521553 | E5RHJ8* | 309 | 168 |
Gene Properties
Recurrent Mutations
All 551 amino-acid changes on canonical ENST00000523629 · 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 RUNX1T1 · cell line vs tissue
For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in RUNX1T1 – 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 |
|---|---|---|
| Chronic Myelogenous Leukemia | 4/25 16% | 0/0 0% |
| T-Cell Non-Hodgkins Lymphoma | 2/26 8% | 0/0 0% |
| T-Lymphoblastic Leukemia | 3/40 8% | 0/0 0% |
| Oral Cavity Carcinoma | 4/54 7% | 0/0 0% |
| Melanoma | 7/210 3% | 126/1899 7% |
| Endometrial Carcinoma | 5/42 12% | 36/612 6% |
| Squamous Cell Lung Carcinoma | 10/57 18% | 42/810 5% |
| Non-Small Cell Lung Carcinoma | 35/304 12% | 54/1390 4% |
| Acute Myeloid Leukemia | 3/90 3% | 0/0 0% |
| Colorectal Carcinoma | 18/143 13% | 83/3239 3% |
| Esophageal Squamous Cell Carcinoma | 5/51 10% | 70/2550 3% |
| Neuroendocrine Tumour | 13/154 8% | 7/577 1% |
| Other Solid Cancers | 0/94 0% | 42/1515 3% |
| Small Cell Lung Carcinoma | 0/9 0% | 19/752 3% |
| Gastric Carcinoma | 3/74 4% | 40/1809 2% |
| Head and Neck Carcinoma | 6/85 7% | 29/1574 2% |
| Glioblastoma | 2/98 2% | 0/0 0% |
| Hepatocellular Carcinoma | 0/46 0% | 42/2210 2% |
| Bladder Carcinoma | 2/58 3% | 16/956 2% |
| Cervical Carcinoma | 0/35 0% | 8/422 2% |
| Ovarian Carcinoma | 4/109 4% | 13/998 1% |
| Hodgkins Lymphoma | 1/16 6% | 1/122 1% |
| Non-Cancerous | 0/104 0% | 12/830 1% |
| Esophageal Carcinoma | 0/23 0% | 10/769 1% |
| Plasma Cell Myeloma | 4/44 9% | 0/305 0% |
| Biliary Tract Carcinoma | 1/54 2% | 9/950 1% |
| Pancreatic Carcinoma | 3/89 3% | 14/1611 1% |
| Other Sarcomas | 2/69 3% | 5/699 1% |
| Adrenocortical Carcinoma | 0/3 0% | 1/112 1% |
| Gastrointestinal Stromal Tumour | 0/0 0% | 1/133 1% |
Mutation Distribution
Where RUNX1T1 is mutated · all tissues, split by cell line vs tissue
How many mutations in RUNX1T1 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 7,715 mutations in RUNX1T1
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 |
|---|