ADRB3

Gene Information
 
Gene Symbol
ADRB3
 
Aliases
BETA3AR
 
Entrez Gene ID
155
 
Gene Name
Adrenoceptor beta 3
 
Chromosomal Location
8p11.23
 
HGNC ID
288
 
Summary
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]
 
RefSeq DNA
 
RefSeq mRNA
  e!Ensembl
Gene
Transcript  
Protein

SNPs

SNP
SNP ID
Associated disease
References
W64R Premature pubarche

Gene Ontology (GO)

GO ID Ontology Function Evidence Reference
GO:0002025 Biological process Norepinephrine-epinephrine-mediated vasodilation involved in regulation of systemic arterial blood pressure IBA 21873635
GO:0002032 Biological process Desensitization of G protein-coupled receptor signaling pathway by arrestin IDA 15123695
GO:0005975 Biological process Carbohydrate metabolic process TAS 2570461
GO:0006091 Biological process Generation of precursor metabolites and energy TAS 2570461
GO:0006112 Biological process Energy reserve metabolic process TAS 1718744
Protein Information
 
Protein Name
Beta-3 adrenergic receptor, adrenergic, beta-3-, receptor, beta-3 adrenoceptor, beta-3 adrenoreceptor
 
Function
Beta-adrenergic receptors mediate the catecholamine-induced activation of adenylate cyclase through the action of G proteins. Beta-3 is involved in the regulation of lipolysis and thermogenesis
 
Refseq Proteins
 
UniProt
 
PDB
Pathways
 
KEGG
 
Reactome
 

Calcium signaling pathway
cGMP-PKG signaling pathway
Neuroactive ligand-receptor interaction
Thermogenesis
Regulation of lipolysis in adipocytes
Renin secretion
Salivary secretion

 

Adrenoceptors
G alpha (s) signalling events
ADORA2B mediated anti-inflammatory cytokines production

     
References
 
 
PubMed ID Disease SNP/Mutation Study population Ethnicity Age of study population Type of sample
Premature pubarche 
W64R  
Total Patients- 40 children (PP: 6 boys and 34 girls), 29 adolescent girls (hyperandrogenism), Controls- Women:15 (white) 
Black, White, Asian-white, Black-white 
Group 1 - 4.6-10.75 years, Group 2 - 10.4-18 years  
Blood
Premature pubarche 
W64R  
Total Patients- Premature Pubarche- 63 children (8 boys and 55 girls), Hirsutism/ oligomenorrhea- 33 girls 
AfricanAmerican, Caucasian-AfricanAmerican, Oriental-Caucasian.  
before age 8 years in girls and before age 9.5 years in boys. 
Blood

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