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 | 1,031 | 163 | 852 |
| Samples | 338 | 64 | 266 |
| Peptides | 263 | 49 | 215 |
Function
NPR3 · Natriuretic peptide receptor 3
This gene encodes one of three natriuretic peptide receptors. Natriutetic peptides are small peptides which regulate blood volume and pressure, pulmonary hypertension, and cardiac function as well as some metabolic and growth processes. The product of this gene encodes a natriuretic peptide receptor responsible for clearing circulating and extracellular natriuretic peptides through endocytosis of the receptor. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Feb 2011].
Isoforms & Proteins
5 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 231 amino-acid changes on canonical ENST00000265074 · 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 NPR3 · cell line vs tissue
For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in NPR3 – 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 | 3/40 8% | 0/0 0% |
| Chronic Myelogenous Leukemia | 1/25 4% | 0/0 0% |
| Hodgkins Lymphoma | 0/16 0% | 5/122 4% |
| Non-Small Cell Lung Carcinoma | 20/304 7% | 22/1390 2% |
| Gastrointestinal Stromal Tumour | 0/0 0% | 3/133 2% |
| Endometrial Carcinoma | 3/42 7% | 9/612 1% |
| Melanoma | 6/210 3% | 32/1899 2% |
| Other Solid Cancers | 1/94 1% | 25/1515 2% |
| Colorectal Carcinoma | 12/143 8% | 41/3239 1% |
| Squamous Cell Lung Carcinoma | 3/57 5% | 8/810 1% |
| Gastric Carcinoma | 0/74 0% | 23/1809 1% |
| Esophageal Carcinoma | 0/23 0% | 9/769 1% |
| Acute Myeloid Leukemia | 1/90 1% | 0/0 0% |
| Head and Neck Carcinoma | 1/85 1% | 16/1574 1% |
| Cervical Carcinoma | 1/35 3% | 3/422 1% |
| Plasma Cell Myeloma | 1/44 2% | 2/305 1% |
| Bladder Carcinoma | 1/58 2% | 6/956 1% |
| Small Cell Lung Carcinoma | 0/9 0% | 5/752 1% |
| Other Sarcomas | 2/69 3% | 3/699 0% |
| Germ Cell Tumour | 0/25 0% | 1/169 1% |
| Biliary Tract Carcinoma | 0/54 0% | 5/950 1% |
| Osteosarcoma | 0/45 0% | 1/166 1% |
| Glioma | 0/52 0% | 10/2127 0% |
| Ovarian Carcinoma | 2/109 2% | 3/998 0% |
| Hepatocellular Carcinoma | 0/46 0% | 9/2210 0% |
| Non-Cancerous | 0/104 0% | 3/830 0% |
| Neuroendocrine Tumour | 1/154 1% | 1/577 0% |
| B-Cell Non-Hodgkins Lymphoma | 0/88 0% | 7/2534 0% |
| Breast Carcinoma | 1/144 1% | 8/3264 0% |
| Medulloblastoma | 0/0 0% | 1/450 0% |
Mutation Distribution
Where NPR3 is mutated · all tissues, split by cell line vs tissue
How many mutations in NPR3 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 1,031 mutations in NPR3
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 |
|---|