|
Symbol Name ID |
Wls
wntless WNT ligand secretion mediator MGI:1915401 |
| Darker colors indicate more annotations |
| Human Phenotypes | Micrognathia |
Microcephaly |
Broad distal phalanx of finger |
Long fingers |
Hypoplasia of the phalanges of the toes |
Toe syndactyly |
Ectrodactyly |
Sacral dimple |
Scoliosis |
| Disease(s) Associated with WLS | |||||||||
| Zaki syndrome |
| Mouse Phenotypes | abnormal neurocranium morphology |
abnormal viscerocranium morphology |
abnormal tooth morphology |
short fibula |
short tibia |
decreased caudal vertebrae number |
abnormal tendon morphology |
abnormal skeleton morphology |
abnormal ligament morphology |
chondrodystrophy |
delayed cranial suture closure |
delayed bone ossification |
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| Availability | Mouse Genotype | ||||||||||||
| Wlsem1Jgg/Wlsem1Jgg | |||||||||||||
| Wlsem2Jgg/Wlsem2Jgg | |||||||||||||
| Wlstm1.1Whsu/Wlstm1.1Whsu H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
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| Wlstm1Xzg/Wlstm1Xzg Tg(Msx2-cre)5Rem/0 (conditional) |
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| Wlstm1Xzg/Wlstm1Xzg Tg(Prrx1-cre)1Cjt/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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