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Pex10em1Lutzy
Endonuclease-mediated Allele Detail
Summary
Symbol: Pex10em1Lutzy
Name: peroxisomal biogenesis factor 10; endonuclease-mediated mutation 1, Cathy Lutz
MGI ID: MGI:6836733
Synonyms: Pex10C286C,G287G,H288D
Gene: Pex10  Location: Chr4:155151487-155156863 bp, + strand  Genetic Position: Chr4, 86.17 cM
Alliance: Pex10em1Lutzy page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Endonuclease-mediated (Humanized sequence)
Mutation:    Nucleotide substitutions
 
Mutation detailsCRISPR/cas9 genome editing is used to generate the H288D missense mutation. (CAT to GAT). The H288D missense mutation that corresponds to the human H310D clinical mutation associated with Zellweger syndrome and peroxisome biogenesis disorders type 6A and 6B .Additionally, the following silent nucleotide changes were included to improve efficiency by preventing guide reassociation and retargeting of the modified allele with CRISPR/Cas9 (C286C [TGT to TGC] and G287G [GGC to GGT]). (J:94077)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Pex10 Mutation:  15 strains or lines available
References
Original:  J:94077 Mutant Mouse Regional Resource Centers, Information obtained from the Mutant Mouse Regional Resource Centers (MMRRC). Unpublished. 2004-2015;
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
05/07/2024
MGI 6.23
The Jackson Laboratory