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Plpp3tm3.1Stw
Targeted Allele Detail
Summary
Symbol: Plpp3tm3.1Stw
Name: phospholipid phosphatase 3; targeted mutation 3.1, Colin L Stewart
MGI ID: MGI:3723634
Synonyms: Ppap2bdeltafloxed
Gene: Plpp3  Location: Chr4:105014544-105089961 bp, + strand  Genetic Position: Chr4, 49.18 cM
Alliance: Plpp3tm3.1Stw page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:125025
Parent Cell Line:  W9.5/W95 (ES Cell)
Strain of Origin:  129S1/Sv-Oca2+ Tyr+ Kitl+
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsExons 3 and 4 were removed by cre-mediated recombination. Recombination was confirmed by Southern blot. These exons encode the second outer loop that is essential for catalytic activity and the tripeptide RGA thought to function in cell-cell interactions. This allele is expected to behave as a null. (J:125025)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 3 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 Plpp3 Mutation:  32 strains or lines available
References
Original:  J:125025 Escalante-Alcalde D, et al., Generation of a conditional Ppap2b/Lpp3 null allele. Genesis. 2007 Jul;45(7):465-9
All:  3 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