Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
186
Gene name Gene Name - the full gene name approved by the HGNC.
Angiotensin II receptor type 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
AGTR2
Synonyms (NCBI Gene) Gene synonyms aliases
AT2, ATGR2, MRX88
Disease Acronyms (UniProt) Disease acronyms from UniProt database
MRX88
Chromosome Chromosome number
X
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
Xq23
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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 information of associated ontologies with gene provided by GO database.
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 ISS
GO:0002018 Process Renin-angiotensin regulation of aldosterone production IEA
GO:0004930 Function G protein-coupled receptor activity IBA 21873635
GO:0004945 Function Angiotensin type II receptor activity IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
300034 338 ENSG00000180772
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Mental retardation non-syndromic X-linked intellectual disability GenCC
Neurodevelopmental Disorders X-linked complex neurodevelopmental disorder GenCC
Diabetes Diabetes GWAS
Associations from Text Mining
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