Genetic diseases of renal phosphate handling.

doi:10.1093/ndt/gfu217

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Article

Genetic diseases of renal phosphate handling.

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association - 1 Sept 2014

Wagner Carsten A, Rubio-Aliaga Isabel, Biber Jürg, Hernando Nati

Abstract excerpt

UNLABELLED: Renal control of systemic phosphate homeostasis is critical as evident from inborn and acquired diseases causing renal phosphate wasting. At least three transport proteins are responsible for renal phosphate reabsorption: NAPI-IIa (SLC34A1), NAPI-IIc (SLC34A3) and PIT-2 (SLC20A2). These transporters are highly regulated by various cellular mechanisms and factors including acid-base status, electrolyte...

Topics

Fibroblast Growth Factor-23
Genetic Markers
Genetic Predisposition to Disease
Humans
Kidney Diseases
Phosphates

Source

Open in PubMed

Identifiers

PMID: 25165185
DOI: 10.1093/ndt/gfu217

Genes

FGF23
MEPE
PHEX
PTH

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

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