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| Nomenclature |
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Symbol:
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Pgrtm2(cre)Lyd
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Name:
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progesterone receptor;
targeted mutation 2, John P Lydon
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MGI ID: |
MGI:3576366 |
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Synonyms: |
PRCre, PR-Cre |
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Gene:
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Pgr
Location:
Chr9:8900419-8965425 bp, + strand
Genetic Position: Chr9,
2.46 cM
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Mutation origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:97321
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Parent Cell Line:
| R1 (ES Cell) |
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Strain of Origin:
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(129X1/SvJ x 129S1/Sv)F1-Kitl+
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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 recombinase cDNA was inserted into exon 1. An untranslated region was created immediately 5' of the cDNA by mutating the ATG codon for the B isoform to prevent an in-frame fusion from the N-terminal of the cre cDNA to the remaining 120 amino acids at the N-terminal end of the endogenous gene. A loxP-flanked neo was inserted 3' of the cre insertion. RNase protection analysis demonstrated that cre transcription was restricted to progestin target tissues, including the uterus, mammary gland and oviduct/ovary. (J:97321)
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Recombinase activity
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Driver:
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Pgr
Summary of all recombinase alleles
driven by Pgr.
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MGI has not yet included tissue activity data for this allele in any anatomical systems.
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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 Pgr Mutation:
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6 strains or lines available |
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| References |
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Original: |
J:97321
Soyal SM et al.,
"Cre-mediated recombination in cell lineages that express the progesterone receptor."
Genesis 2005 Feb;41(2):58-66
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All: |
37 reference(s)
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