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 | Cystic hygroma |
Increased nuchal translucency |
Short neck |
Small for gestational age |
Intrauterine growth retardation |
Disease(s) Associated with MUSK | |||||
fetal akinesia deformation sequence syndrome 1 |
Mouse Phenotypes | growth/size/body region phenotype |
decreased body weight |
weight loss |
decreased body size |
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Availability | Mouse Genotype | ||||
Musktm1.2Ics/Musktm1.2Ics | |||||
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 03/19/2024 MGI 6.23 |
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