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| Nomenclature |
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Symbol:
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Bsndtm1.1Suc
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Name:
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Bartter syndrome, infantile, with sensorineural deafness (Barttin);
targeted mutation 1.1, Shinichi Uchida
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MGI ID: |
MGI:5285211 |
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Synonyms: |
BsndR8L |
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Gene:
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Bsnd
Location:
Chr4:106483456-106492283 bp, - strand
Genetic Position: Chr4,
49.67 cM
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Mutation
origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:175265
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Parent Cell Line:
| J1 (ES Cell) |
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Strain of Origin:
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129S4/SvJae
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Mutation
description |
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Allele
Type: | |
Targeted (knock-in) |
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Mutation: | |
Insertion |
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Mutation details: Cre-mediated recombination removed the neo cassette downstream of the modified exon 1 with the R8L substitution and removed by cre-mediated recombination. (J:175265)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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Disease models
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available |
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Carrying any Bsnd Mutation:
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4 strains or lines available |
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| References |
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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
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All: |
1 reference(s)
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Analysis Tools
