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Symbol
Name
ID

Chrng
cholinergic receptor, nicotinic, gamma polypeptide
MGI:87895

Phenotype annotations related to muscle

Darker colors indicate more annotations

Human Phenotypes	Weakness of facial musculature	Camptodactyly of toe	Knee flexion contracture	Flexion contracture	Arthrogryposis multiplex congenita	Camptodactyly	Multiple joint contractures	Congenital diaphragmatic hernia	Amyoplasia	Diaphragmatic eventration
Disease(s) Associated with CHRNG
contractures, pterygia, and spondylocarpotarsal fusion syndrome

Mouse Phenotypes		abnormal skeletal muscle fiber morphology	increased variability of skeletal muscle fiber size	abnormal diaphragm morphology	thin diaphragm muscle	abnormal muscle physiology
Availability	Mouse Genotype	abnormal skeletal muscle fiber morphology	increased variability of skeletal muscle fiber size	abnormal diaphragm morphology	thin diaphragm muscle	abnormal muscle physiology
	Chrng^tm1Mtak/Chrng^tm1Mtak
	Chrng^{tm2(Chrne)Vwi}/Chrng^{tm2(Chrne)Vwi}

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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