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Pex10m1Nisw
Chemically induced Allele Detail
Summary
Symbol: Pex10m1Nisw
Name: peroxisomal biogenesis factor 10; mutation 1, Lee Niswander
MGI ID: MGI:5638060
Synonyms: Pex10CY
Gene: Pex10  Location: Chr4:155151487-155156863 bp, + strand  Genetic Position: Chr4, 86.17 cM
Alliance: Pex10m1Nisw page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsENU induced a single base pair change from G to A, that results in the amino acid substitution of a cysteine for tyrosine at position 294 (C294Y), which disrupts the second zinc RING finger binding domain. (J:216140)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 18 assay results
In Structures Affected by this Mutation: 2 anatomical structure(s)
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:216140 Hanson MG, et al., Peripheral nervous system defects in a mouse model for peroxisomal biogenesis disorders. Dev Biol. 2014 Nov 1;395(1):84-95
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
12/10/2024
MGI 6.24
The Jackson Laboratory