Symbol Name ID |
Tfam
transcription factor A, mitochondrial MGI:107810 |
Darker colors indicate more annotations |
Human Phenotypes | Ascites |
Abdominal distention |
Failure to thrive |
Cachexia |
Intrauterine growth retardation |
Disease(s) Associated with TFAM | |||||
amyotrophic lateral sclerosis | |||||
mitochondrial DNA depletion syndrome 15 |
Mouse Phenotypes | increased heart weight |
enlarged heart |
slow postnatal weight gain |
weight loss |
decreased body size |
postnatal growth retardation |
distended abdomen |
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Availability | Mouse Genotype | |||||||
Tfamtm1.1Lrsn/Tfamtm1.1Lrsn | ||||||||
Tfamtm1.1Ncdl/Tfamtm1.1Ncdl Tg(KRT14-cre)1Amc/0 (conditional) |
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Tfamtm1Lrsn/Tfamtm1Lrsn Tg(Ckmm-cre)1Lrsn/0 (conditional) |
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Tfamtm1Lrsn/Tfamtm1Lrsn Tg(Myhca-cre)1Lrsn/0 (conditional) |
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Myl1tm1(cre)Sjb/Myl1+ Tfamtm1Lrsn/Tfamtm1Lrsn (conditional) |
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Cnptm1(cre)Kan/Cnp+ 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 04/16/2024 MGI 6.23 |
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