Gene Gene information from NCBI Gene database.
Entrez ID 186
Gene name Angiotensin II receptor type 2
Gene symbol AGTR2
Synonyms (NCBI Gene)
AT2ATGR2MRX88
Chromosome X
Chromosome location Xq23
Summary The protein encoded by this gene belongs to the G-protein coupled receptor 1 family, and functions as a receptor for angiotensin II. It is an intergral membrane protein that is highly expressed in fetus and in neonates, but scantily in adult tissues, exce
miRNA miRNA information provided by mirtarbase database.
45
miRTarBase ID miRNA Experiments Reference
MIRT019253 hsa-miR-148b-3p Microarray 17612493
MIRT021590 hsa-miR-142-3p Microarray 17612493
MIRT022332 hsa-miR-124-3p Microarray 18668037
MIRT528494 hsa-miR-548p PAR-CLIP 22012620
MIRT528493 hsa-miR-378j PAR-CLIP 22012620
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
52
GO ID Ontology Definition Evidence Reference
GO:0001974 Process Blood vessel remodeling TAS 17159080
GO:0001991 Process Regulation of systemic arterial blood pressure by circulatory renin-angiotensin IEA
GO:0001991 Process Regulation of systemic arterial blood pressure by circulatory renin-angiotensin ISS
GO:0002033 Process Angiotensin-mediated vasodilation involved in regulation of systemic arterial blood pressure IEA
GO:0002035 Process Brain renin-angiotensin system IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
300034 338 ENSG00000180772
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P50052
Protein name Type-2 angiotensin II receptor (Angiotensin II type-2 receptor) (AT2 receptor)
Protein function Receptor for angiotensin II, a vasoconstricting peptide (PubMed:28379944, PubMed:29967536, PubMed:31899086, PubMed:8185599). Signals primarily via a non-canonical G-protein- and beta-arrestin independent pathways (PubMed:28379944). Cooperates wi
PDB 5UNF , 5UNG , 5UNH , 5XJM , 6JOD , 7C6A , 7JNI
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 61 318 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: In adult, highly expressed in myometrium with lower levels in adrenal gland and fallopian tube. Expressed in the cerebellum. Very highly expressed in fetal kidney and intestine. {ECO:0000269|PubMed:12089445}.
Sequence
Sequence length 363
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
7
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
AGTR2-related disorder Likely benign; Conflicting classifications of pathogenicity; Uncertain significance; Benign rs387906503, rs35474657, rs2520575070, rs150381803, rs5191 RCV003964797
RCV003914827
RCV003961549
RCV003923206
RCV003915056
Intellectual disability, X-linked 88 Benign; Likely benign rs121917810 RCV000604777
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma Associate 37991139
Alzheimer Disease Associate 37813091
Arthritis Rheumatoid Associate 29038523
Atrial Fibrillation Associate 16043935, 32383373
Cardiomegaly Associate 12453540
Cardiomyopathy Dilated Associate 35618744
Cardiomyopathy Hypertrophic Associate 21163866
Cardiovascular Diseases Associate 12453540, 28792482
Coronary Restenosis Associate 34065198
Coronary Restenosis Stimulate 34065198