Symbol Name ID |
Musk
muscle, skeletal, receptor tyrosine kinase MGI:103581 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Stillbirth |
Disease(s) Associated with MUSK | |
fetal akinesia deformation sequence syndrome 1 |
Mouse Phenotypes | mortality/aging |
premature death |
neonatal lethality, complete penetrance |
postnatal lethality, incomplete penetrance |
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Availability | Mouse Genotype | ||||
Musktm1.1Vwi/Musktm1.1Vwi | |||||
Musktm1.2Ics/Musktm1.2Ics | |||||
Musktm1Gdy/Musktm1Gdy | |||||
Musktm2Vwi/Musktm2Vwi | * | ||||
Musktm1.1Vwi/Musktm2Vwi | |||||
Musktm1Vwi/Musktm1Vwi Tg(Ckmm-cre)5Khn/0 (conditional) |
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Musktm1Vwi/Musktm1.1Vwi Tg(Ckmm-cre)5Khn/0 (conditional) |
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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last database update 09/03/2024 MGI 6.24 |
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