AGTR2 (angiotensin II receptor type 2)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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186 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Angiotensin II receptor type 2 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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AGTR2 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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AT2, ATGR2, MRX88 |
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Chromosome
Chromosome number
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X |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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Xq23 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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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 |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| 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
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| 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 |
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| Sequence length | 363 | ||||||||||
| Interactions | View interactions | ||||||||||
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Associated diseases
Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
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