|
Symbol Name ID |
Pex5
peroxisomal biogenesis factor 5 MGI:1098808 |
| Darker colors indicate more annotations |
| Human Phenotypes | Joint contracture of the hand |
Contractures of the large joints |
Camptodactyly |
Hypotonia |
Generalized hypotonia |
Muscle weakness |
Skeletal muscle atrophy |
| Disease(s) Associated with PEX5 | |||||||
| peroxisome biogenesis disorder 2A | |||||||
| rhizomelic chondrodysplasia punctata type 5 |
| Mouse Phenotypes | muscle weakness |
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| Availability | Mouse Genotype | |
| Pex5tm1Baes/Pex5tm1Baes | ||
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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