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Symbol Name ID |
Prdm5
PR domain containing 5 MGI:1918029 |
| Darker colors indicate more annotations |
| Human Phenotypes | Joint hypermobility |
Recurrent fractures |
| Disease(s) Associated with PRDM5 | ||
| brittle cornea syndrome 2 |
| Mouse Phenotypes | abnormal bone structure |
abnormal bone collagen fibril morphology |
decreased bone mineral content |
decreased bone mineral density of femur |
decreased compact bone volume |
decreased trabecular bone volume |
decreased bone volume |
abnormal osteoblast morphology |
delayed bone ossification |
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| Availability | Mouse Genotype | |||||||||
| Prdm5Gt(AV0702)Wtsi/Prdm5Gt(AV0702)Wtsi | ||||||||||
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 04/16/2024 MGI 6.23 |
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