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| Nomenclature |
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Symbol:
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Pex7tm1Rjaw
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Name:
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peroxisomal biogenesis factor 7;
targeted mutation 1, Ronald JA Wanders
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MGI ID: |
MGI:3052739 |
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Synonyms: |
Pex7- |
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Gene:
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Pex7
Location:
Chr10:19859929-19907689 bp, - strand
Genetic Position: Chr10,
9.16 cM, cytoband A3
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Mutation
origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:92346
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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 (Reporter) |
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Mutation: | |
Disruption caused by insertion of vector |
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Mutation details: A beta galactosidase reporter gene fused with a neomycin phosphotransferas gene (beta geo cassette) replaced exon 3 and parts of introns 2 and 3 of the gene. (J:92346)
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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 Pex7 Mutation:
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3 strains or lines available |
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| References |
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Original: |
J:92346
Brites P et al.,
"Impaired neuronal migration and endochondral ossification in Pex7 knockout mice: a model for rhizomelic chondrodysplasia punctata."
Hum Mol Genet 2003 Sep 15;12(18):2255-67
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All: |
1 reference(s)
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Analysis Tools
