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Symbol
Name
ID

Fxr1
FMR1 autosomal homolog 1
MGI:104860

Phenotype annotations related to muscle

Darker colors indicate more annotations

Human Phenotypes	Neonatal hypotonia	EMG: myopathic abnormalities	Proximal muscle weakness	Type 1 muscle fiber predominance	Z-band streaming	Centrally nucleated skeletal muscle fibers	Fatty replacement of skeletal muscle	Minicore myopathy
Disease(s) Associated with FXR1	Neonatal hypotonia	EMG: myopathic abnormalities	Proximal muscle weakness	Type 1 muscle fiber predominance	Z-band streaming	Centrally nucleated skeletal muscle fibers	Fatty replacement of skeletal muscle	Minicore myopathy
congenital myopathy 9A
congenital myopathy 9B

Mouse Phenotypes		abnormal myocardial fiber morphology	disorganized myocardium	abnormal muscle development
Availability	Mouse Genotype	abnormal myocardial fiber morphology	disorganized myocardium	abnormal muscle development
	Fxr1^tm1.2Dln/Fxr1^tm1.2Dln
	Fxr1^tm1Dln/Fxr1^tm1Dln

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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