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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 |
Short stature |
| Disease(s) Associated with WLS | ||
| Zaki syndrome |
| Mouse Phenotypes | abnormal tooth morphology |
cleft palate |
abnormal nose morphology |
decreased body size |
postnatal growth retardation |
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| Availability | Mouse Genotype | |||||
| Wlstm1.1Arte/Wlstm1.1Arte Krt14tm1(cre)Wbm/Krt14+ (conditional) |
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| Wlstm1.1Whsu/Wlstm1.1Whsu H2az2Tg(Wnt1-cre)11Rth/H2az2+ (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 05/07/2024 MGI 6.23 |
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