Symbol Name ID |
Tafazzin
tafazzin, phospholipid-lysophospholipid transacylase MGI:109626 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal mitochondrial morphology |
Disease(s) Associated with TAFAZZIN | |
Barth syndrome |
Mouse Phenotypes | azoospermia |
abnormal spermatocyte morphology |
abnormal mitochondrial morphology |
disorganized mitochondrial cristae |
abnormal mitochondrial shape |
decreased mitochondrial size |
increased mitochondrial number |
abnormal cellular respiration |
abnormal respiratory electron transport chain |
abnormal mitochondrial physiology |
increased mitochondrial fission |
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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/Y Tg(myl7.L-cre)1118Tmhn/0 (conditional) |
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 04/23/2024 MGI 6.23 |
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