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 | 750 | 116 | 629 |
| Samples | 355 | 74 | 279 |
| Peptides | 284 | 49 | 241 |
Function
CNST · Consortin, connexin sorting protein
Targeting of numerous transmembrane proteins to the cell surface is thought to depend on their recognition by cargo receptors that interact with the adaptor machinery for anterograde traffic at the distal end of the Golgi complex. Consortin (CNST) is an integral membrane protein that acts as a binding partner of connexins, the building blocks of gap junctions, and acts as a trans-Golgi network (TGN) receptor involved in connexin targeting to the plasma membrane and recycling from the cell surface (del Castillo et al., 2010 [PubMed 19864490]).[supplied by OMIM, Jun 2010].
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 275 amino-acid changes on canonical ENST00000366513 · 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 CNST · cell line vs tissue
For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in CNST – 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% |
| Acute Myeloid Leukemia | 4/90 4% | 0/0 0% |
| Glioblastoma | 4/98 4% | 0/0 0% |
| T-Cell Non-Hodgkins Lymphoma | 1/26 4% | 0/0 0% |
| Gastrointestinal Stromal Tumour | 0/0 0% | 5/133 4% |
| Endometrial Carcinoma | 5/42 12% | 17/612 3% |
| Thymic Epithelial Tumor | 0/0 0% | 1/39 3% |
| Non-Small Cell Lung Carcinoma | 20/304 7% | 22/1390 2% |
| Melanoma | 7/210 3% | 43/1899 2% |
| Squamous Cell Lung Carcinoma | 4/57 7% | 13/810 2% |
| Bladder Carcinoma | 0/58 0% | 15/956 2% |
| Colorectal Carcinoma | 9/143 6% | 34/3239 1% |
| Gastric Carcinoma | 0/74 0% | 21/1809 1% |
| Small Cell Lung Carcinoma | 0/9 0% | 8/752 1% |
| Esophageal Squamous Cell Carcinoma | 0/51 0% | 17/2550 1% |
| Ovarian Carcinoma | 3/109 3% | 4/998 0% |
| Other Solid Cancers | 0/94 0% | 10/1515 1% |
| Biliary Tract Carcinoma | 0/54 0% | 6/950 1% |
| Breast Carcinoma | 7/144 5% | 13/3264 0% |
| Hepatocellular Carcinoma | 0/46 0% | 13/2210 1% |
| Germ Cell Tumour | 0/25 0% | 1/169 1% |
| Cervical Carcinoma | 0/35 0% | 2/422 0% |
| Burkitts Lymphoma | 1/32 3% | 0/196 0% |
| Mesothelioma | 1/62 2% | 0/165 0% |
| Non-Cancerous | 0/104 0% | 4/830 0% |
| Glioma | 0/52 0% | 8/2127 0% |
| Head and Neck Carcinoma | 1/85 1% | 5/1574 0% |
| Ewings Sarcoma | 0/63 0% | 1/262 0% |
| Kidney Carcinoma | 2/85 2% | 3/1862 0% |
| Other Sarcomas | 0/69 0% | 2/699 0% |
Mutation Distribution
Where CNST is mutated · all tissues, split by cell line vs tissue
How many mutations in CNST 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 750 mutations in CNST
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 |
|---|