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Symbol Name ID |
Tfam
transcription factor A, mitochondrial MGI:107810 |
| Darker colors indicate more annotations |
| Human Phenotypes | Jaundice |
| Disease(s) Associated with TFAM | |
| mitochondrial DNA depletion syndrome 15 |
| Mouse Phenotypes | decreased subcutaneous adipose tissue amount |
abnormal keratinocyte differentiation |
increased keratinocyte proliferation |
absent sebaceous gland |
progressive hair loss |
decreased hair follicle number |
abnormal hair cycle catagen phase |
thick epidermis |
abnormal keratinocyte physiology |
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| Availability | Mouse Genotype | |||||||||
| Tfamtm1.1Ncdl/Tfamtm1.1Ncdl Tg(KRT14-cre)1Amc/0 (conditional) |
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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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