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Symbol Name ID |
Wnt1
wingless-type MMTV integration site family, member 1 MGI:98953 |
| Darker colors indicate more annotations |
| Human Phenotypes | Joint hypermobility |
Bowing of limbs due to multiple fractures |
Recurrent fractures |
Thin ribs |
Scoliosis |
Platyspondyly |
Osteoporosis |
| Disease(s) Associated with WNT1 | |||||||
| osteogenesis imperfecta type 15 | |||||||
| osteoporosis |
| Mouse Phenotypes | abnormal parietal bone morphology |
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| Availability | Mouse Genotype | |
| Wnt1tm1Brd/Wnt1tm1Brd | ||
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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