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Bsndtm1Tjj
Targeted Allele Detail
Nomenclature
Symbol: Bsndtm1Tjj
Name: Bartter syndrome, infantile, with sensorineural deafness (Barttin); targeted mutation 1, Thomas J Jentsch
MGI ID: MGI:3826849
Synonyms: Bsndlox
Gene: Bsnd  Location: Chr4:106483456-106492283 bp, - strand  Genetic Position: Chr4, 49.67 cM
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
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View phenotypes for all genotypes (concatenated display).
Disease models
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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:  4 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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/18/2014
MGI 5.20
The Jackson Laboratory