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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Fxr1
FMR1 autosomal homolog 1
MGI:104860
14 phenotypes from 3 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Fxr1tm1.2Dln/Fxr1tm1.2Dln
involves: 129P2/OlaHsd * C57BL/6
abnormal muscle development J:91191
abnormal myocardial fiber morphology J:91191
abnormal skin vasculature morphology J:91191
neonatal lethality, complete penetrance J:91191
Fxr1tm1Dln/Fxr1tm1Dln
involves: 129P2/OlaHsd * C57BL/6
abnormal gait J:91191
abnormal muscle development J:91191
decreased grip strength J:91191
disorganized myocardium J:91191
postnatal growth retardation J:91191
premature death J:91191
short stride length J:91191
small heart J:91191
small lung J:91191
small spleen J:91191
small testis J:91191
Fxr1tm1Drad/Fxr1tm1Drad
Not Specified
neonatal lethality, complete penetrance J:206028

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
04/30/2024
MGI 6.23
The Jackson Laboratory