About   Help   FAQ
Bsndtm1Tjj
Targeted Allele Detail
Summary
Symbol: Bsndtm1Tjj
Name: barttin CLCNK type accessory beta subunit; targeted mutation 1, Thomas J Jentsch
MGI ID: MGI:3826849
Synonyms: Bsndlox
Gene: Bsnd  Location: Chr4:106340653-106349440 bp, - strand  Genetic Position: Chr4, 49.67 cM
Alliance: Bsndtm1Tjj page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:143314
Parent Cell Line:  MPI-II (ES Cell)
Strain of Origin:  129S2/SvPas
Mutation
description
Allele Type:    Targeted (Conditional ready, No functional change)
Mutation:    Insertion
    Exon 2 was flanked by loxP sites. (J:143314)
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Disease models
Loading...
Expression
In Structures Affected by this Mutation: 2 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Bsnd Mutation:  16 strains or lines available
References
Original:  J:143314 Rickheit G, et al., Endocochlear potential depends on Cl- channels: mechanism underlying deafness in Bartter syndrome IV. EMBO J. 2008 Nov 5;27(21):2907-17
All:  1 reference(s)

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
05/28/2024
MGI 6.13
The Jackson Laboratory