Symbol Name ID |
Clcn7
chloride channel, voltage-sensitive 7 MGI:1347048 |
Darker colors indicate more annotations |
Human Phenotypes | Elevated serum acid phosphatase |
Hypocalcemia |
Disease(s) Associated with CLCN7 | ||
autosomal dominant osteopetrosis 2 |
Mouse Phenotypes | abnormal autophagy |
enhanced autophagy |
increased circulating parathyroid hormone level |
increased circulating alkaline phosphatase level |
abnormal chloride level |
|
Availability | Mouse Genotype | |||||
Clcn7tm2Tjj/Clcn7tm2Tjj | ||||||
Clcn7tm4.1Tjj/Clcn7tm4.1Tjj | ||||||
Clcn7tm5.1Tjj/Clcn7tm5.1Tjj | ||||||
Clcn7tm1.1Mjec/Clcn7+ | ||||||
Clcn7tm1.1Teti/Clcn7+ |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 08/02/2024 MGI 6.24 |
|
|