CHRM1

Cholinergic receptor muscarinic 1 P11229 ACM1_HUMAN
Protein Coding Chr 11 11q12.3 Swiss-Prot reviewed Entrez 1128
Mutations
259
CL 67 · Tissue 189
Samples
246
CL 62 · Tissue 182
Peptides
179
unique mutant peptides
Transcripts
1
isoforms mutated

Stats by Source

Total, split by cell line (COSMIC CL / DepMap / PubMed) vs tissue (COSMIC primary tissue)

How the counts split by source
Stats by Source

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.

TotalCell lineTissue
Mutations25967189
Samples24662182
Peptides17942146

Function

CHRM1 · Cholinergic receptor muscarinic 1

The muscarinic cholinergic receptors belong to a larger family of G protein-coupled receptors. The functional diversity of these receptors is defined by the binding of acetylcholine and includes cellular responses such as adenylate cyclase inhibition, phosphoinositide degeneration, and potassium channel mediation. Muscarinic receptors influence many effects of acetylcholine in the central and peripheral nervous system. The muscarinic cholinergic receptor 1 is involved in mediation of vagally-induced bronchoconstriction and in the acid secretion of the gastrointestinal tract. The gene encoding this receptor is localized to 11q13. [provided by RefSeq, Jul 2008].

Isoforms & Proteins

1 transcript · UniProt mapping is sequence-verified (AA-safe)

About the isoform mapping
Isoforms & Proteins

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.

TranscriptUniProtMutationsPeptides
ENST00000306960 P11229 259 179

Gene Properties

Type
Protein Coding
Chromosome
11
Cytoband
11q12.3
Entrez ID
Aliases
HM1M1M1R

Recurrent Mutations

All 179 amino-acid changes on canonical ENST00000306960 · needle height = samples · drag the mini-map to zoom

What this lollipop shows
Recurrent Mutations

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 CHRM1 · cell line vs tissue

How this frequency is counted
Cancer-type mutation frequency

For each cancer type, the fraction of samples that carry at least one missense/complex mutation anywhere in CHRM1 – 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 typeCell linesTissue samples
Chordoma
0/7 0%
2/13 15%
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
T-Lymphoblastic Leukemia
2/40 5%
0/0 0%
Endometrial Carcinoma
0/42 0%
14/612 2%
Glioblastoma
2/98 2%
0/0 0%
Melanoma
8/210 4%
21/1899 1%
Colorectal Carcinoma
9/143 6%
33/3239 1%
Gastric Carcinoma
0/74 0%
23/1809 1%
Neuroendocrine Tumour
7/154 5%
1/577 0%
Cervical Carcinoma
2/35 6%
3/422 1%
Other Solid Cancers
5/94 5%
8/1515 1%
Squamous Cell Lung Carcinoma
3/57 5%
3/810 0%
Hepatocellular Carcinoma
1/46 2%
14/2210 1%
Non-Small Cell Lung Carcinoma
8/304 3%
2/1390 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
13/2550 1%
Bladder Carcinoma
0/58 0%
5/956 1%
Glioma
0/52 0%
10/2127 0%
Esophageal Carcinoma
0/23 0%
3/769 0%
Head and Neck Carcinoma
3/85 4%
3/1574 0%
Ewings Sarcoma
0/63 0%
1/262 0%
Plasma Cell Myeloma
0/44 0%
1/305 0%
Breast Carcinoma
1/144 1%
9/3264 0%
Other Sarcomas
0/69 0%
2/699 0%
Biliary Tract Carcinoma
0/54 0%
2/950 0%
Ovarian Carcinoma
1/109 1%
1/998 0%
Prostate Carcinoma
0/13 0%
3/2105 0%
Neuroblastoma
2/87 2%
0/1331 0%
Pancreatic Carcinoma
0/89 0%
2/1611 0%
B-Cell Non-Hodgkins Lymphoma
3/88 3%
0/2534 0%
B-Lymphoblastic Leukemia
2/55 4%
1/2640 0%

Mutation Distribution

Where CHRM1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in CHRM1 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

GTEx Portal ↗
About the expression data
GTEx Expression

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 259 mutations in CHRM1

About the mutation list
Mutations

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.

IDSampleTranscriptAA Change CDSTypeSourceMutant PeptideWild-type Peptide