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Bsndtm1.1Suc
Targeted Allele Detail
Nomenclature
Symbol: Bsndtm1.1Suc
Name: Bartter syndrome, infantile, with sensorineural deafness (Barttin); targeted mutation 1.1, Shinichi Uchida
MGI ID: MGI:5285211
Synonyms: BsndR8L
Gene: Bsnd  Location: Chr4:106483456-106492283 bp, - strand  Genetic Position: Chr4, 49.67 cM
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:175265
Parent Cell Line:  J1 (ES Cell)
Strain of Origin:  129S4/SvJae
Mutation
description
Allele Type:    Targeted
Mutation:    Insertion
 
Mutation details
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:175265 Nomura N, et al., Generation and analyses of R8L barttin knockin mouse. Am J Physiol Renal Physiol. 2011 Aug;301(2):F297-307
All:  2 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