|
Symbol Name ID |
Bsnd
barttin CLCNK type accessory beta subunit MGI:2153465 |
| Darker colors indicate more annotations |
| Human Phenotypes | Polydipsia |
Intellectual disability |
Hyporeflexia |
Motor delay |
| Disease(s) Associated with BSND | ||||
| Bartter disease type 4a |
| Mouse Phenotypes | cochlear outer hair cell degeneration |
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| Availability | Mouse Genotype | |
| Bsndtm1Tjj/Bsndtm1Tjj Tg(Sox10-cre)1Wdr/0 (conditional) |
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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 04/23/2024 MGI 6.23 |
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