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Symbol Name ID |
Wls
wntless WNT ligand secretion mediator MGI:1915401 |
| Darker colors indicate more annotations |
| Human Phenotypes | Congenital diaphragmatic hernia |
Hypertonia |
Spastic gait |
Hypotonia |
| Disease(s) Associated with WLS | ||||
| Zaki syndrome |
| Mouse Phenotypes | abnormal muscle development |
abnormal tendon morphology |
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| Availability | Mouse Genotype | ||
| Wlstm1Xzg/Wlstm1Xzg Tg(Msx2-cre)5Rem/0 (conditional) |
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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 04/23/2024 MGI 6.23 |
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