About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Stk39tm2.1Arte
targeted mutation 2.1, TaconicArtemis
MGI:5770425
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Stk39tm2.1Arte/Stk39tm2.1Arte involves: C57BL/6J MGI:5804131


Genotype
MGI:5804131
hm1
Allelic
Composition
Stk39tm2.1Arte/Stk39tm2.1Arte
Genetic
Background
involves: C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Stk39tm2.1Arte mutation (0 available); any Stk39 mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• mice exhibit a lower augmentation index (AIx, defined as augmentation pressure/pulse pressure) relative to wild-type controls (21.1 +/- 1.0 % versus 35.0 +/- 2.1 %), indicating a reduction in arterial stiffness
• mice display a significantly lower left ventricular mass, as determined by the weight of the left ventricle and septum combined (LV+S) expressed as a % of body weight
• mice exhibit a lower diastolic pressure time decay constant (taubourgeois, an index of vascular resistance) relative to wild-type controls (0.44 +/- 0.01 s versus 0.56 +/- 0.02 s), suggesting a reduction in vascular tone
• pulse waveform analysis revealed a significant decrease in augmentation pressure (SBP minus anacrotic notch pressure), in dicrotic notch pressure, and in MAP (1/3 SBP plus 2/3 DBP) relative to wild-type controls
• however, pulse pressure (SBP minus DBP) is normal
• mice exhibit lower heart rates than wild-type controls
• under general anesthesia, mean arterial blood pressure (MAP) is 20 mmHg lower than in wild-type controls
• under general anesthesia, diastolic blood pressure (DBP) is 20 mmHg lower than in wild-type controls
• under general anesthesia, systolic blood pressure (SBP) is 20 mmHg lower than in wild-type controls
• mice display a reduction in vascular contractility, as indicated by their lower augmentation index (AIx) and a decrease in the diastolic pressure decay time constant (taubourgeois)

homeostasis/metabolism
• mice exhibit mild hypomagnesemia
• mice exhibit mild hypokalemia
• mice exhibit a marked reduction in creatinine normalized urinary calcium levels
• however, plasma calcium levels are not significantly altered
• after switching from a 3% w/w to a 0.03% w/w salt (Na) diet, mice show a significant increase in urinary Na+ excretion relative to similarly treated wild-type controls, indicating salt wasting

renal/urinary system
N
• mice exhibit no remodeling of renal tubules, despite a striking reduction in the phosphorylated forms of NCC and NKCC2 in the distal convoluted (DCT) and thick ascending limb (TAL) tubules
• mice exhibit a marked reduction in creatinine normalized urinary calcium levels
• however, plasma calcium levels are not significantly altered
• after switching from a 3% w/w to a 0.03% w/w salt (Na) diet, mice show a significant increase in urinary Na+ excretion relative to similarly treated wild-type controls, indicating salt wasting

muscle
• mice display a reduction in vascular contractility, as indicated by their lower augmentation index (AIx) and a decrease in the diastolic pressure decay time constant (taubourgeois)

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Gitelman syndrome DOID:0050450 OMIM:263800
J:224087





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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
12/10/2024
MGI 6.24
The Jackson Laboratory