Rpe65tm1.1(cre/ERT2)Kser
Targeted Allele Detail
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Symbol: |
Rpe65tm1.1(cre/ERT2)Kser |
Name: |
retinal pigment epithelium 65; targeted mutation 1.1, Philip Kiser |
MGI ID: |
MGI:6501720 |
Gene: |
Rpe65 Location: Chr3:159304812-159330958 bp, + strand Genetic Position: Chr3, 82.52 cM, cytoband H4
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Alliance: |
Rpe65tm1.1(cre/ERT2)Kser page
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Germline Transmission: |
Earliest citation of germline transmission:
J:310003
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Parent Cell Line: |
Other (see notes) (ES Cell)
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Strain of Origin: |
C57BL/6
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Allele Type: |
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Targeted (Inducible, Recombinase) |
Inducer: |
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tamoxifen |
Mutation: |
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Insertion
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Rpe65tm1.1(cre/ERT2)Kser expression driven by
1 gene
Knock-in expression driven by:
Organism |
Driver Gene |
Note |
mouse |
Rpe65 (MGI:98001) |
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Mutation details: The targeting construct was designed to fuse a P2A self-cleaving peptide sequence and a cre/ERT2 sequence in frame at the 3' of exon 14 of the retinal pigment epithelium 65 (Rpe65) gene. The cre-ERT2 fusion gene contains a Cre recombinase fused to a human estrogen receptor ligand binding domain. A frt-flanked neomycin resistance (neo) cassette was placed immediately after the non-coding exon 15. This construct was electroporated into C57BL/6 FLP-derived iTL BF1 embryonic stem (ES) cells. The Neo cassette in the targeting sequence was removed during ES clone expansion.
(J:310003)
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Activity: |
Tissue activity of this recombinase allele
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Driver:
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Rpe65
(mouse)
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Original: |
J:310003 Choi EH, et al., An inducible Cre mouse for studying roles of the RPE in retinal physiology and disease. JCI Insight. 2021 May 10;6(9) |
All: |
3 reference(s) |
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