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Phenotypes Associated with This Genotype
Genotype
MGI:6389011
Allelic
Composition
Kcnj8em1Nich/Kcnj8+
Genetic
Background
involves: C57BL/6J * CBA/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kcnj8em1Nich mutation (0 available); any Kcnj8 mutation (34 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• minor decrease in survival
• minor decrease in survival

cardiovascular system
• increase in aortic diameters, ranging from 15% to 70% increases around the proximal aorta
• ventricular myocyte hypertrophy
• cardiomegaly results from cellular hypertrophy
• 1.7-fold increase in heart weight
• approximate 2-fold increase in left ventricle mass
• 4 of 5 mice show aortic stenosis
• cardiac output is about 65% higher
• echocardiography shows an approximate 2-fold increase in left ventricle mass, dilated left ventricle chamber diameters with increases in left ventricle posterior wall and intraventricular septal thickness, increased cardiac output, increased rate of left ventricle emptying
• however, relative wall thickness and fractional shortening are not different
• 4 of 5 mice show aortic insufficiency
• anesthetized 3-month old mice show a reduction of both systolic and diastolic basal blood pressures
• the effect of pinacidil administration on blood pressure is severely blunted
• approximate 30-mmHg decreases in blood pressure at both night and day, although the difference is not significant during the daytime
• enhanced basal K(ATP) conductance in vascular smooth muscle
• carotid arterial diameters across a full range of physiological pressures are increased, indicating dilated, compliant arterial vessels

muscle
• ventricular myocyte hypertrophy
• enhanced basal K(ATP) conductance in vascular smooth muscle
• carotid arterial diameters across a full range of physiological pressures are increased, indicating dilated, compliant arterial vessels

nervous system
• whole-cell patch-clamp recordings show an approximate 5-fold higher basal potassium conductance in acutely isolated smooth muscle cells
• the effect of pinacidil, the K(ATP) channel opener, is blunted in vascular smooth muscle cells (does not provoke increase in conductance) and subsequent application of the K(ATP) channel inhibitor, glibenclamide, is less effective

growth/size/body
• cardiomegaly results from cellular hypertrophy
• 1.7-fold increase in heart weight

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
hypertrichotic osteochondrodysplasia Cantu type DOID:0060569 OMIM:239850
J:281903


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
11/05/2024
MGI 6.24
The Jackson Laboratory