ADRB1

Adrenoceptor beta 1 P08588 ADRB1_HUMAN
Protein Coding Chr 10 10q25.3 Swiss-Prot reviewed Entrez 153
Mutations
221
CL 56 · Tissue 151
Samples
206
CL 54 · Tissue 147
Peptides
158
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
Mutations22156151
Samples20654147
Peptides15838114

Function

ADRB1 · Adrenoceptor beta 1

The adrenergic receptors (subtypes alpha 1, alpha 2, beta 1, and beta 2) are a prototypic family of guanine nucleotide binding regulatory protein-coupled receptors that mediate the physiological effects of the hormone epinephrine and the neurotransmitter norepinephrine. Beta-1 adrenoceptors are predominately located in the heart. Specific polymorphisms in this gene have been shown to affect the resting heart rate and can be involved in heart failure. [provided by RefSeq, Sep 2019].

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
ENST00000369295 P08588 221 158

Gene Properties

Type
Protein Coding
Chromosome
10
Cytoband
10q25.3
Entrez ID
Aliases
ADRB1RB1ARBETA1ARFNSS2RHR

Recurrent Mutations

All 158 amino-acid changes on canonical ENST00000369295 · 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 ADRB1 · 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 ADRB1 – 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
Chronic Myelogenous Leukemia
2/25 8%
0/0 0%
Oral Cavity Carcinoma
4/54 7%
0/0 0%
T-Lymphoblastic Leukemia
2/40 5%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
5/133 4%
Endometrial Carcinoma
3/42 7%
7/612 1%
Colorectal Carcinoma
8/143 6%
29/3239 1%
Glioblastoma
1/98 1%
0/0 0%
Gastric Carcinoma
2/74 3%
17/1809 1%
Melanoma
5/210 2%
15/1899 1%
Mesothelioma
2/62 3%
0/165 0%
Cervical Carcinoma
0/35 0%
4/422 1%
Bladder Carcinoma
1/58 2%
7/956 1%
Thyroid Gland Carcinoma
0/45 0%
12/1592 1%
Other Solid Cancers
0/94 0%
8/1515 1%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Burkitts Lymphoma
1/32 3%
0/196 0%
Non-Small Cell Lung Carcinoma
3/304 1%
4/1390 0%
Neuroendocrine Tumour
2/154 1%
1/577 0%
Biliary Tract Carcinoma
0/54 0%
4/950 0%
Other Sarcomas
3/69 4%
0/699 0%
Esophageal Squamous Cell Carcinoma
2/51 4%
8/2550 0%
Esophageal Carcinoma
1/23 4%
2/769 0%
Ovarian Carcinoma
3/109 3%
1/998 0%
Head and Neck Carcinoma
0/85 0%
6/1574 0%
Non-Cancerous
0/104 0%
3/830 0%
Plasma Cell Myeloma
1/44 2%
0/305 0%
Squamous Cell Lung Carcinoma
0/57 0%
2/810 0%
Hepatocellular Carcinoma
2/46 4%
3/2210 0%
Medulloblastoma
0/0 0%
1/450 0%
B-Cell Non-Hodgkins Lymphoma
2/88 2%
2/2534 0%

Mutation Distribution

Where ADRB1 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ADRB1 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 221 mutations in ADRB1

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