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Symbol Name ID |
Fxr1
FMR1 autosomal homolog 1 MGI:104860 |
| Darker colors indicate more annotations |
| Human Phenotypes | Decreased fetal movement |
| Disease(s) Associated with FXR1 | |
| congenital myopathy 9B |
| Mouse Phenotypes | decreased grip strength |
abnormal gait |
short stride length |
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| Availability | Mouse Genotype | |||
| Fxr1tm1Dln/Fxr1tm1Dln | ||||
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 04/30/2024 MGI 6.23 |
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