AT2: Receptor for angiotensin II. Cooperates with MTUS1 to inhibit ERK2 activation and cell proliferation. Defects in AGTR2 are the cause of mental retardation X- linked type 88 (MRX88). Mental retardation is characterized by significantly below average general intellectual functioning associated with impairments in adaptative behavior and manifested during the developmental period. Belongs to the G-protein coupled receptor 1 family.
Protein type: Membrane protein, integral; Receptor, GPCR; Membrane protein, multi-pass; GPCR, family 1
Chromosomal Location of Human Ortholog: Xq22-q23
Cellular Component: perinuclear region of cytoplasm; integral to plasma membrane; extracellular region; plasma membrane
Molecular Function: protein binding; receptor antagonist activity; angiotensin type II receptor activity; peptide hormone binding; transcription factor binding
Biological Process: positive regulation of phosphoprotein phosphatase activity; regulation of transcription factor import into nucleus; negative regulation of icosanoid secretion; positive regulation of nitric oxide biosynthetic process; negative regulation of heart rate; negative regulation of nerve growth factor receptor signaling pathway; positive regulation of transcription, DNA-dependent; renin-angiotensin regulation of aldosterone production; dopamine biosynthetic process; positive regulation of vasodilation; angiotensin mediated vasodilation involved in regulation of systemic arterial blood pressure; cerebellar cortex development; regulation of systemic arterial blood pressure by circulatory renin-angiotensin; cell surface receptor linked signal transduction; regulation of blood pressure; positive regulation of cell proliferation; inflammatory response; cellular sodium ion homeostasis; positive regulation of nitric-oxide synthase activity; response to organic nitrogen; negative regulation of blood vessel endothelial cell migration; brain renin-angiotensin system; G-protein coupled receptor protein signaling pathway; negative regulation of fibroblast proliferation; blood vessel remodeling; G-protein signaling, coupled to cGMP nucleotide second messenger; brain development; negative regulation of cell growth; nitric oxide mediated signal transduction; positive regulation of cytokine secretion
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