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Symbol
Name
ID
Bsnd
barttin CLCNK type accessory beta subunit
MGI:2153465
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Intellectual disability
Hyporeflexia
Motor delay
Disease(s) Associated with BSND
Bartter disease type 4a

Mouse Phenotypes
cochlear outer hair cell degeneration
Availability Mouse Genotype
Bsndtm1Tjj/Bsndtm1Tjj
Tg(Sox10-cre)1Wdr/0  (conditional)

Contributing Projects:
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
02/11/2020
MGI 6.14
The Jackson Laboratory