Mouse Genome Informatics
ht
    Mesttm1Masu/Mest+
Not Specified
Key:
phenotype observed in females WTSI Wellcome Trust Sanger Institute
phenotype observed in males EuPh Europhenome
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
• subtle alteration in the pattern of trabeculation when mutant allele inherited paternally

muscle
• subtle alteration in the pattern of trabeculation when mutant allele inherited paternally

cellular

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