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Pld4mpc96H
Chemically induced Allele Detail
Summary
Symbol: Pld4mpc96H
Name: phospholipase D family member 4; muta-ped-c3pde 96, Harwell
MGI ID: MGI:5791986
Gene: Pld4  Location: Chr12:112727089-112735420 bp, + strand  Genetic Position: Chr12, 61.2 cM
Alliance: Pld4mpc96H page
Mutation
origin
Strain of Origin:  C57BL/6J
Project Collection: Harwell ENU Mutagenesis
Mutation
description
Allele Type:    Chemically induced (ENU) (Not Specified)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced a C to T point mutation that results in the amino acid substitution of phenylalanine for leucine at position 158 (L158F). (J:234901)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
Find Mice (IMSR)
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
Carrying any Pld4 Mutation:  26 strains or lines available
References
Original:  J:234901 Potter PK, et al., Novel gene function revealed by mouse mutagenesis screens for models of age-related disease. Nat Commun. 2016;7:12444
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
11/19/2024
MGI 6.24
The Jackson Laboratory