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Symbol Name ID |
Clpp
caseinolytic mitochondrial matrix peptidase proteolytic subunit MGI:1858213 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Cubitus valgus |
Scoliosis |
Osteoporosis |
| Disease(s) Associated with CLPP | ||||
| Perrault syndrome |
| Mouse Phenotypes | abnormal bone structure |
decreased bone mineral content |
decreased bone mineral density |
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| Availability | Mouse Genotype | |||
| Clpptm1a(EUCOMM)Wtsi/Clpptm1a(EUCOMM)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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