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Symbol
Name
ID

Musk
muscle, skeletal, receptor tyrosine kinase
MGI:103581

Phenotype annotations related to mortality/aging

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

Human Phenotypes	Stillbirth
Disease(s) Associated with MUSK	Stillbirth
fetal akinesia deformation sequence syndrome 1

Mouse Phenotypes		mortality/aging	premature death	neonatal lethality, complete penetrance	postnatal lethality, incomplete penetrance
Availability	Mouse Genotype	mortality/aging	premature death	neonatal lethality, complete penetrance	postnatal lethality, incomplete penetrance
	Musk^tm1.1Vwi/Musk^tm1.1Vwi
	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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