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Symbol
Name
ID
Tfam
transcription factor A, mitochondrial
MGI:107810
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Abnormality of eye movement
Disease(s) Associated with TFAM
Huntington's disease

Mouse Phenotypes
absent optic nerve
Availability Mouse Genotype
Tfamtm1.1Lrsn/Tfamtm1.1Lrsn

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
05/14/2024
MGI 6.23
The Jackson Laboratory