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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Klhl3+
wild type
MGI:3702653
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Klhl3tm1.1Esoh/Klhl3+ involves: C57BL/6 MGI:5646380
ht2
Klhl3tm1.1Slin/Klhl3+ Not Specified MGI:6393411


Genotype
MGI:5646380
ht1
Allelic
Composition
Klhl3tm1.1Esoh/Klhl3+
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Klhl3tm1.1Esoh mutation (0 available); any Klhl3 mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• significantly greater increase in systolic blood pressure on a high salt diet
• blood pressure on a normal salt diet is similar to controls

homeostasis/metabolism

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
pseudohypoaldosteronism DOID:4479 J:214330




Genotype
MGI:6393411
ht2
Allelic
Composition
Klhl3tm1.1Slin/Klhl3+
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

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

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

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





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last database update
03/25/2025
MGI 6.24
The Jackson Laboratory