Symbol Name ID |
Fxr1
FMR1 autosomal homolog 1 MGI:104860 |
Darker colors indicate more annotations |
Human Phenotypes | Death in infancy |
Disease(s) Associated with FXR1 | |
congenital myopathy 9A |
Mouse Phenotypes | premature death |
neonatal lethality, complete penetrance |
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Availability | Mouse Genotype | ||
Fxr1tm1.2Dln/Fxr1tm1.2Dln | |||
Fxr1tm1Dln/Fxr1tm1Dln | |||
Fxr1tm1Drad/Fxr1tm1Drad |
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 |
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