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| Nomenclature |
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Symbol:
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Spentm2.1Hon
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Name:
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SPEN homolog, transcriptional regulator (Drosophila);
targeted mutation 2.1, Tasuku Honjo
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MGI ID: |
MGI:3710413 |
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Synonyms: |
MINT cko, Mintf |
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Gene:
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Spen
Location:
Chr4:141467890-141538597 bp, - strand
Genetic Position: Chr4,
74.26 cM, cytoband E1
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Mutation
origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:121523
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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 (Floxed/Frt) |
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Mutation: | |
Insertion |
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Mutation details: ES cells containing the Spentm2Hon allele were infected with adenovirus expressing cre at low levels. This resulted in removal of the neomycin expression vector and left exon 11 flanked by loxP sites. (J:121523)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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| References |
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Original: |
J:121523
Yabe D et al.,
"Generation of a conditional knockout allele for mammalian Spen protein Mint/SHARP."
Genesis 2007 May;45(5):300-6
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All: |
2 reference(s)
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Analysis Tools
