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Symbol Name ID |
Lama5
laminin, alpha 5 MGI:105382 |
| Darker colors indicate more annotations |
| Human Phenotypes | Thickened nuchal skin fold |
| Disease(s) Associated with LAMA5 | |
| bent bone dysplasia syndrome 2 |
| Mouse Phenotypes | abnormal placental labyrinth vasculature morphology |
abnormal embryo size |
incomplete rostral neuropore closure |
abnormal extraembryonic tissue morphology |
abnormal placenta morphology |
decreased placental labyrinth size |
abnormal trophoblast layer morphology |
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| Availability | Mouse Genotype | |||||||
| Lama5Gt1Jhm/Lama5Gt1Jhm | ||||||||
| Lama5tm1Jhm/Lama5tm1Jhm | ||||||||
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 03/24/2026 MGI 6.24 |
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