|
Symbol Name ID |
Clcn5
chloride channel, voltage-sensitive 5 MGI:99486 |
| Darker colors indicate more annotations |
| Human Phenotypes | Umbilical hernia |
Short stature |
| Disease(s) Associated with CLCN5 | ||
| Dent disease | ||
| low molecular weight proteinuria with hypercalciuric nephrocalcinosis | ||
| X-linked recessive hypophosphatemic rickets |
| Mouse Phenotypes | abnormal tooth development |
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| Availability | Mouse Genotype | |
| Clcn5tm1Gug/Y | ||
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 04/09/2024 MGI 6.23 |
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