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Symbol
Name
ID
Tafazzin
tafazzin, phospholipid-lysophospholipid transacylase
MGI:109626
Phenotype annotations related to cardiovascular system
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Endocardial fibroelastosis
Dilated cardiomyopathy
Hypertrophic cardiomyopathy
Increased left ventricular end-diastolic volume
Tricuspid regurgitation
Arrhythmia
Congestive heart failure
Disease(s) Associated with TAFAZZIN
Barth syndrome

Mouse Phenotypes
cardiovascular system phenotype
abnormal myocardial fiber morphology
abnormal heart morphology
globular heart
enlarged heart
abnormal heart left ventricle morphology
dilated heart left ventricle
dilated cardiomyopathy
decreased cardiac muscle contractility
decreased heart left ventricle muscle contractility
abnormal heart echocardiography feature
Availability Mouse Genotype
Gt(ROSA)26Sortm37(H1/tetO-RNAi:Tafazzin)Arte/Gt(ROSA)26Sor+
Tafazzintm1Dost/Y *
Gt(ROSA)26Sortm37(H1/tetO-RNAi:Tafazzin)Arte/?
Tafazzinem1Xfa/Tafazzinem1Xfa
Tg(myl7.L-cre)1118Tmhn/0  (conditional)
Tafazzinem1Xfa/Y
Tg(myl7.L-cre)1118Tmhn/0  (conditional)

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
08/02/2024
MGI 6.24
The Jackson Laboratory