Symbol Name ID |
Tfam
transcription factor A, mitochondrial MGI:107810 |
Darker colors indicate more annotations |
Human Phenotypes | Hypertyrosinemia |
Hypermethioninemia |
Hyperbilirubinemia |
Conjugated hyperbilirubinemia |
Hypoalbuminemia |
Elevated circulating hepatic transaminase concentration |
Elevated circulating alkaline phosphatase concentration |
Hypoglycemia |
Microvesicular hepatic steatosis |
4-hydroxyphenylacetic aciduria |
4-Hydroxyphenylpyruvic aciduria |
Ascites |
Disease(s) Associated with TFAM | ||||||||||||
mitochondrial DNA depletion syndrome 15 |
Mouse Phenotypes | decreased insulin secretion |
abnormal circulating insulin level |
decreased dopamine level |
abnormal enzyme/coenzyme level |
increased insulin sensitivity |
increased glutathione peroxidase activity |
increased physiological sensitivity to xenobiotic |
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Availability | Mouse Genotype | |||||||
Tfamtm1Lrsn/Tfamtm1Lrsn Tg(Ckmm-cre)1Lrsn/0 (conditional) |
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Tfamtm1Lrsn/Tfamtm1Lrsn Tg(Ins2-cre)25Mgn/0 (conditional) |
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Slc6a3tm1(cre)Lrsn/Slc6a3+ Tfamtm1Lrsn/Tfamtm1Lrsn (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 08/02/2024 MGI 6.24 |
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