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Article

AVPR2 variants and V2 vasopressin receptor function in nephrogenic diabetes insipidus.

Kidney international - 1 Dec 1998

Wildin R S, Cogdell D E, Valadez V

Abstract excerpt

BACKGROUND: The AVPR2 gene encodes the type 2 vasopressin receptor, a member of the vasopressin/oxytocin receptor subfamily of G protein-coupled receptors. Disruption of AVPR2 causes X-linked congenital nephrogenic diabetes insipidus (NDI), yet the functional significance of most gene sequence variations found in association with NDI has not been proven. The large number of naturally occurring AVPR2 mutations...

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Source

Identifiers

PMID: 9853256
DOI: 10.1046/j.1523-1755.1998.00214.x

Genes

AVPR2
AVP

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Vasopressin type 2 receptor V88M mutation: molecular basis of partial and complete nephrogenic diabetes insipidus.Semantic proximity Read ↗

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Vasopressin receptor mutations and nephrogenic diabetes insipidus.Semantic proximity Read ↗

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Molecular and cellular defects in nephrogenic diabetes insipidus.Semantic proximity Read ↗

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