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Phenotypes Associated with This Genotype
Genotype
MGI:6393415
Allelic
Composition
Klhl3tm1.1Slin/Klhl3tm1.1Slin
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Klhl3tm1.1Slin mutation (0 available); any Klhl3 mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system

homeostasis/metabolism
• mice show decreased fractional excretion of potassium
• hyperchloremic metabolic acidosis
• secondary hyporeninemia
• mice show a blunted diuretic response to treatment with furosemide (NKCC2 inhibitor), showing decreased fractional excretion of sodium, potassium and chloride
• mice show an increased diuretic response to hydrochlorothiazide (NCC inhibitor), showing increased fractional excretion of sodium, potassium and chloride

renal/urinary system
• mice show decreased fractional excretion of potassium

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
pseudohypoaldosteronism DOID:4479 J:284284


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory