Bptftm1.2Cwu
Targeted Allele Detail
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Symbol: |
Bptftm1.2Cwu |
Name: |
bromodomain PHD finger transcription factor; targeted mutation 1.2, Carl Wu |
MGI ID: |
MGI:3841298 |
Synonyms: |
BptfdeltaExon2 |
Gene: |
Bptf Location: Chr11:106923907-107022953 bp, - strand Genetic Position: Chr11, 70.11 cM
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Alliance: |
Bptftm1.2Cwu page
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Allele Type: |
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Targeted (Null/knockout) |
Mutation: |
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Intragenic deletion
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Mutation details: A loxP site was inserted upstream of exon 2, and a frt-flnaked neomycin cassette and a downstream loxP site was inserted downstream of exon 2. Transient cre recombinase expression removed exon 2 and the neomycin cassette. Despite the deletion, mRNA from the locus was still detected in heterozygous tissues including the brain and testis. Sequencing of exons 1-8 revealed the mRNA was out of frame indicating that this is a loss-of-function allele. This was confirmed through allelic complementation assays and by a lack of protein detectable in immunoblot assays.
(J:147414)
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View phenotypes and curated references for all genotypes (concatenated display).
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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
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Carrying any Bptf Mutation: |
157 strains or lines available
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Original: |
J:147414 Landry J, et al., Essential role of chromatin remodeling protein Bptf in early mouse embryos and embryonic stem cells. PLoS Genet. 2008 Oct;4(10):e1000241 |
All: |
1 reference(s) |
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