Porcntm1.2Vdv
Targeted Allele Detail
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Symbol: |
Porcntm1.2Vdv |
Name: |
porcupine O-acyltransferase; targeted mutation 1, Ignatia B Van den Veyver |
MGI ID: |
MGI:5435557 |
Synonyms: |
Porcn-ex3-7del |
Gene: |
Porcn Location: ChrX:8060087-8072764 bp, - strand Genetic Position: ChrX, 3.7 cM
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Alliance: |
Porcntm1.2Vdv page
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Germline Transmission: |
Earliest citation of germline transmission:
J:186934
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Parent Cell Line: |
Not Specified (ES Cell)
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Strain of Origin: |
129S5/SvEvBrd
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Allele Type: |
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Targeted (Null/knockout) |
Mutations: |
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Insertion, Intragenic deletion
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Mutation details: A loxP site was inserted upstream of exon 3 and a loxP site and FRT flanked neo cassette were inserted downstream of exon 7. Flp mediated recombination removed the neo cassette. Cre mediated recombination removed exons 3 - 7.
(J:186934)
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Generation of Porcn targeted alleles |
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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 Porcn Mutation: |
18 strains or lines available
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Original: |
J:186934 Liu W, et al., Deletion of Porcn in mice leads to multiple developmental defects and models human focal dermal hypoplasia (Goltz syndrome). PLoS One. 2012;7(3):e32331 |
All: |
1 reference(s) |
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