ADRB3

Adrenoceptor beta 3 P13945 ADRB3_HUMAN
Protein Coding Chr 8 8p11.23 Swiss-Prot reviewed Entrez 155
Mutations
216
CL 31 · Tissue 167
Samples
199
CL 31 · Tissue 162
Peptides
166
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
Mutations21631167
Samples19931162
Peptides16629130

Function

ADRB3 · Adrenoceptor beta 3

The protein encoded by this gene belongs to the family of beta adrenergic receptors, which mediate catecholamine-induced activation of adenylate cyclase through the action of G proteins. This receptor is located mainly in the adipose tissue and is involved in the regulation of lipolysis and thermogenesis. Obesity and bodyweight-related disorders are correlated with certain polymorphisms in three subtypes of beta-adrenoceptor, among them, the ADRB3 gene.[provided by RefSeq, Oct 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
ENST00000345060 P13945 216 166

Gene Properties

Type
Protein Coding
Chromosome
8
Cytoband
8p11.23
Entrez ID
Aliases
BETA3AR

Recurrent Mutations

All 166 amino-acid changes on canonical ENST00000345060 · 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 ADRB3 · 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 ADRB3 – 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
Unknown
0/10 0%
1/29 3%
T-Lymphoblastic Leukemia
1/40 2%
0/0 0%
Gastrointestinal Stromal Tumour
0/0 0%
3/133 2%
Oral Cavity Carcinoma
1/54 2%
0/0 0%
Hodgkins Lymphoma
1/16 6%
1/122 1%
Gastric Carcinoma
0/74 0%
26/1809 1%
Neuroendocrine Tumour
3/154 2%
7/577 1%
Small Cell Lung Carcinoma
0/9 0%
10/752 1%
Acute Myeloid Leukemia
1/90 1%
0/0 0%
Colorectal Carcinoma
3/143 2%
29/3239 1%
Endometrial Carcinoma
1/42 2%
5/612 1%
Non-Small Cell Lung Carcinoma
2/304 1%
13/1390 1%
Thyroid Gland Carcinoma
0/45 0%
10/1592 1%
Ovarian Carcinoma
3/109 3%
3/998 0%
Rhabdomyosarcoma
0/33 0%
1/171 1%
Squamous Cell Lung Carcinoma
2/57 4%
2/810 0%
Mesothelioma
1/62 2%
0/165 0%
Non-Cancerous
0/104 0%
4/830 0%
Melanoma
1/210 0%
8/1899 0%
Esophageal Squamous Cell Carcinoma
1/51 2%
10/2550 0%
Ewings Sarcoma
1/63 2%
0/262 0%
Other Solid Cancers
1/94 1%
4/1515 0%
Biliary Tract Carcinoma
0/54 0%
3/950 0%
B-Lymphoblastic Leukemia
3/55 5%
5/2640 0%
Esophageal Carcinoma
0/23 0%
2/769 0%
Head and Neck Carcinoma
0/85 0%
4/1574 0%
Cervical Carcinoma
0/35 0%
1/422 0%
Hepatocellular Carcinoma
1/46 2%
4/2210 0%
Medulloblastoma
0/0 0%
1/450 0%
Prostate Carcinoma
1/13 8%
3/2105 0%

Mutation Distribution

Where ADRB3 is mutated · all tissues, split by cell line vs tissue

Mutation counts by tissue
Mutation Distribution

How many mutations in ADRB3 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 40 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 216 mutations in ADRB3

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