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Phenotypes Associated with This Genotype
Genotype
MGI:2677277
Allelic
Composition
Mesttm1Masu/Mest+
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mesttm1Masu mutation (0 available); any Mest mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• increased thickness and reduced density of compact myocardium when mutat allele inherited paternally, similar to that seen in human cardiomyopathy ventricular noncompaction (J:79223)
• increased thickness and reduced density of compact myocardium when mutat allele inherited paternally, similar to that seen in human cardiomyopathy ventricular noncompaction (J:79223)
• subtle alteration in the pattern of trabeculation when mutant allele inherited paternally (J:79223)
• subtle alteration in the pattern of trabeculation when mutant allele inherited paternally (J:79223)

muscle
• subtle alteration in the pattern of trabeculation when mutant allele inherited paternally (J:79223)
• subtle alteration in the pattern of trabeculation when mutant allele inherited paternally (J:79223)

cellular

Mouse Models of Human Disease
OMIM ID Ref(s)
Barth Syndrome; BTHS 302060 J:79223


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
02/02/2016
MGI 6.02
The Jackson Laboratory