Pkhd1tm2.1Cjwa
Targeted Allele Detail
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Symbol: |
Pkhd1tm2.1Cjwa |
Name: |
polycystic kidney and hepatic disease 1; targeted mutation 2.1, Christopher J Ward |
MGI ID: |
MGI:5438325 |
Synonyms: |
Pkhd1Pk(+) |
Gene: |
Pkhd1 Location: Chr1:20128003-20688288 bp, - strand Genetic Position: Chr1, 6.27 cM, cytoband A2-A5
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Alliance: |
Pkhd1tm2.1Cjwa page
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Germline Transmission: |
Earliest citation of germline transmission:
J:187735
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Parent Cell Line: |
Not Specified (ES Cell)
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Strain of Origin: |
129
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Allele Type: |
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Targeted |
Mutation: |
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Insertion
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Mutation details: Pkhd1tm2Cjwa mice were crossed with Tg(Gdf9-cre)5092Coo mice to remove the LSL (loxP-STOP-loxP) cassette leaving a single loxP site in intron 2. Upon removal of the LSL, the gene is reactivated and the expressed protein carries two SV5-Pk epitope tags on its extreme N-terminus. Northern blot analysis reveals the presence of 13 kb, 9 kb, 7.7kb and 7.5kb products identical in length to products generated from the wild-type allele.
(J:187735)
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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 Pkhd1 Mutation: |
225 strains or lines available
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Original: |
J:187735 Bakeberg JL, et al., Epitope-tagged Pkhd1 tracks the processing, secretion, and localization of fibrocystin. J Am Soc Nephrol. 2011 Dec;22(12):2266-77 |
All: |
1 reference(s) |
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