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Symbol
Name
ID
Fxr1
FMR1 autosomal homolog 1
MGI:104860
Phenotype annotations related to mortality/aging
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
Availability Mouse Genotype
Fxr1tm1.2Dln/Fxr1tm1.2Dln
Fxr1tm1Dln/Fxr1tm1Dln
Fxr1tm1Drad/Fxr1tm1Drad

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
04/16/2024
MGI 6.23
The Jackson Laboratory