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| Nomenclature |
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Symbol:
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Baz1btm1Ska
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Name:
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bromodomain adjacent to zinc finger domain, 1B;
targeted mutation 1, Shigeaki Kato
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MGI ID: |
MGI:3850079 |
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Synonyms: |
WSTF- |
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Gene:
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Baz1b
Location:
Chr5:135187264-135246129 bp, + strand
Genetic Position: Chr5,
75.05 cM
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Mutation origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:149990
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Parent Cell Line:
| TT2 (ES Cell) |
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Strain of Origin:
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(C57BL/6NCrlj x CBA/JNCrlj)F1
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Mutation description |
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Allele
Type: | |
Targeted (knock-out) |
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Mutations: | |
Insertion, Intragenic deletion |
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Mutation details: Exon 1 was replaced with a neo cassette. The absence of protein expression was confirmed by western blot analysis on E10.5 embryo extracts. (J:149990)
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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 Baz1b Mutation:
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24 strains or lines available |
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| References |
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Original: |
J:149990
Yoshimura K et al.,
"Distinct function of 2 chromatin remodeling complexes that share a common subunit, Williams syndrome transcription factor (WSTF)."
Proc Natl Acad Sci U S A 2009 Jun 9;106(23):9280-5
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All: |
1 reference(s)
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