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GeneQ14890035· pop 5· linked from 617 articles

Also known as ADHR, DI1, DIR, DIR3, NDI, V2R, arginine vasopressin receptor 2, NDI1

protein-coding gene in the species Homo sapiens

Gene data

AVPR2
Name
arginine vasopressin receptor 2
Type
protein-coding
Chromosome
X
Aliases
ADHR, DI1, DIR, DIR3, NDI, NDI1, V2R

This gene encodes the vasopressin receptor, type 2, also known as the V2 receptor, which belongs to the seven-transmembrane-domain G protein-coupled receptor (GPCR) superfamily, and couples to Gs thus stimulating adenylate cyclase. The subfamily that includes the V2 receptor, the V1a and V1b vasopressin receptors, the oxytocin receptor, and isotocin and mesotocin receptors in non-mammals, is well conserved, though several members signal via other G proteins. All bind similar cyclic nonapeptide hormones. The V2 receptor is expressed in the kidney tubule, predominantly in the distal convoluted tubule and collecting ducts, where its primary property is to respond to the pituitary hormone arginine vasopressin (AVP) by stimulating mechanisms that concentrate the urine and maintain water homeostasis in the organism. When the function of this gene is lost, the disease Nephrogenic Diabetes Insipidus (NDI) results. The V2 receptor is also expressed outside the kidney although its tissue localization is uncertain. When these 'extrarenal receptors' are stimulated by infusion of a V2 selective agonist (dDAVP), a variety of clotting factors are released into the bloodstream. The physiologic importance of this property is not known - its absence does not appear to be detrimental in NDI patients. The gene expression has also been described in fetal lung tissue and lung cancer associated with alternative splicing. [provided by RefSeq, Jul 2008].

via MyGene.info

Gene · Ensembl

arginine vasopressin receptor 2

Symbol
AVPR2
Biotype
Protein coding
Organism
Homo sapiens
Location
Chr X:153,902,531-153,907,169
Strand
Forward (+)
Assembly
GRCh38
View on Ensembl →

via Ensembl · EMBL-EBI

Wikidata facts

Show 5 more facts
HomoloGene ID
20064
genomic start
153167985
genomic end
153172620
cytogenetic location
Xq28
Sources (5)

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