Fxr1 Phenotype Annotations

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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

Allelic Composition Genetic Background	Annotated Term	Reference
Fxr1^tm1.2Dln/Fxr1^tm1.2Dln 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
Fxr1^tm1Dln/Fxr1^tm1Dln 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
Fxr1^tm1Drad/Fxr1^tm1Drad 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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