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Symbol
Name
ID

Musk
muscle, skeletal, receptor tyrosine kinase
MGI:103581

Phenotype annotations related to behavior/neurological

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Decreased fetal movement	Fetal akinesia sequence	Hypernasal speech
Disease(s) Associated with MUSK	Decreased fetal movement	Fetal akinesia sequence	Hypernasal speech
congenital myasthenic syndrome 9
fetal akinesia deformation sequence syndrome 1

Mouse Phenotypes		behavior/neurological phenotype	abnormal motor capabilities/coordination/movement	unresponsive to tactile stimuli	impaired coordination	decreased grip strength	abnormal gait	no spontaneous movement
Availability	Mouse Genotype	behavior/neurological phenotype	abnormal motor capabilities/coordination/movement	unresponsive to tactile stimuli	impaired coordination	decreased grip strength	abnormal gait	no spontaneous movement
	Musk^tm1.2Ics/Musk^tm1.2Ics
	Musk^tm1Gdy/Musk^tm1Gdy
	Musk^tm2Vwi/Musk^tm2Vwi	*
	Musk^tm1.1Vwi/Musk^tm2Vwi
	Musk^tm1Vwi/Musk^tm1Vwi Tg(Ckmm-cre)5Khn/0 (conditional)
	Musk^tm1Vwi/Musk^tm1.1Vwi Tg(Ckmm-cre)5Khn/0 (conditional)

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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