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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Lpar3tm1Jch
targeted mutation 1, Jerold Chun
MGI:3579139
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Lpar3tm1Jch/Lpar3tm1Jch involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3579500


Genotype
MGI:3579500
hm1
Allelic
Composition
Lpar3tm1Jch/Lpar3tm1Jch
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lpar3tm1Jch mutation (1 available); any Lpar3 mutation (13 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
• significant prolongation of pregnancy (20.9 days versus 19.4 days in wildtype), however observed no differences in superovulation, fertilization or decidualization
• homozygous null females exhibited delayed implantation, with implantation sites detectable at E5.5 but not at E4.5
• reduced number of implantation sites even though comparable numbers of blastocysts were available for implantation
• implantation sites in homozygous null uteri were crowded/clustered in the uterine segments proximal to the cervix with 44% of implantation sites containing 2-4 embryos at E10.5
• homozygous null females produced litter sizes of less than 50% compared with wildtype
• E10.5 and E18.5 embryos from homozygous null females were smaller than wildtype, while newborns (at P0) were heavier, possibly resulting from prolonged pregnancy and/or smaller litter size

embryo
• 28% of placentas were shared by two to three embryos at E18.5
• placental hypertrophy

homeostasis/metabolism
• reduced production of PGE2 and PGI2 in uterus during early pregnancy (E3.5) due to significantly reduced levels of COX2 mRNA
• treatment of pregnant homozygous null females (at E3.5) with exogenous PGE2 or PGI2 rescued the delayed implantation defect but not the uneven embryo spacing or the reduction in implantation sites





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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory