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Heritable Phenotypic Marker : urehr1 urea phenotype 1
Primary Identifier  MGI:3712268 Organism  mouse, laboratory
Chromosome  UN Mgi Type  heritable phenotypic marker
description  PHENOTYPE: Homozygotes for this ENU-induced mutation exhibit kidney disease with impaired urinary excretion of metabolism products, polyuria, and kidney alterations. Plasma levels of urea, creatinine, and cholesterol are increased while glucose levels are decreased. Mice show increased food and water intake. [provided by MGI curators]
  • synonyms:
  • urea phenotype 1,
  • urehr1
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Homology

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Gene --> Protein-Protein Interactions

Expression

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Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

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