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Symbol
Name
ID
Bsnd
barttin CLCNK type accessory beta subunit
MGI:2153465
Phenotype annotations related to hearing/vestibular/ear
Darker colors indicate more annotations
Human Phenotypes
Sensorineural hearing impairment
Disease(s) Associated with BSND
Bartter disease type 4a

Mouse Phenotypes
abnormal vestibuloocular dark reflex
collapsed Reissner membrane
cochlear outer hair cell degeneration
abnormal stria vascularis morphology
stria vascularis degeneration
thin stria vascularis
decreased endocochlear potential
increased or absent threshold for auditory brainstem response
absent distortion product otoacoustic emissions
Availability Mouse Genotype
Bsndtm1Tjj/Bsndtm1Tjj
Tg(Sox10-cre)1Wdr/0  (conditional)
Bsndtm1Tjj/Bsndtm1Tjj
Foxg1tm1(cre)Skm/Foxg1+  (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
02/18/2020
MGI 6.14
The Jackson Laboratory