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Article

Mapping of a new candidate locus for uromodulin-associated kidney disease (UAKD) to chromosome 1q41.

Kidney international - 1 Oct 2005

Hodanová Katerina, Majewski Jacek, Kublová Martina, Vyletal Petr, Kalbácová Marie, Stibůrková Blanka, Hůlková Helena, Chagnon Yvon C, Lanouette Christian-Marc, Marinaki Anthony, Fryns Jean-Pierre, Venkat-Raman Gopalakrishnan, Kmoch Stanislav

Abstract excerpt

BACKGROUND: Autosomal-dominant juvenile hyperuricemia, gouty arthritis, medullary cysts, and progressive renal insufficiency are features associated with familial juvenile hyperuricemic nephropathy (FJHN), medullary cystic kidney disease type 1 (MCKD1) and type 2 (MCKD2). MCKD1 has been mapped to chromosome 1q21. FJHN and MCKD2 have been mapped to chromosome 16p11.2. FJHN and MCKD2 are allelic, result from...

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Share to Chromosome Mapping
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 16164624
DOI: 10.1111/j.1523-1755.2005.00560.x

Genes

UMOD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Mapping of a new candidate locus for uromodulin-associated kidney disease (UAKD) to chromosome 1q41.PMID 16164624Read ↗

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The UMOD Locus: Insights into the Pathogenesis and Prognosis of Kidney Disease.Semantic proximity Read ↗

UROMODULIN mutations cause familial juvenile hyperuricemic nephropathy.Semantic proximity Read ↗

A cluster of mutations in the UMOD gene causes familial juvenile hyperuricemic nephropathy with abnormal expression of uromodulin.Semantic proximity Read ↗

Autosomal dominant tubulointerstitial kidney disease caused by uromodulin mutations: seek and you will find.Semantic proximity Read ↗

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