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Pex2tm1Plf
Targeted Allele Detail
Nomenclature
Symbol: Pex2tm1Plf
Name: peroxisomal biogenesis factor 2; targeted mutation 1, Phyllis L Faust
MGI ID: MGI:2180128
Synonyms: PEX2-
Gene: Pex2  Location: Chr3:5560188-5576239 bp, - strand  Genetic Position: Chr3, 1.96 cM
Variable size of and cranial abnormalities in Pex2tm1Plf/Pex2tm1Plf mice

Show the 4 phenotype image(s) involving this allele.

Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:44975
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation details
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Disease models
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Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 3 strains available      Cell Lines: 0 lines available
Carrying any Pex2 Mutation:  4 strains or lines available
References
Original:  J:44975 Faust PL, et al., Targeted deletion of the PEX2 peroxisome assembly gene in mice provides a model for Zellweger syndrome, a human neuronal migration disorder. J Cell Biol. 1997 Dec 1;139(5):1293-305
All:  7 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
07/23/2014
MGI 5.19
The Jackson Laboratory