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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Lpar4
lysophosphatidic acid receptor 4
MGI:1925384
20 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Lpar4tm1.1(KOMP)Vlcg/Y
C57BL/6N-Lpar4tm1.1(KOMP)Vlcg/J 		decreased grip strength J:211773
decreased urine magnesium level J:211773
Lpar4tm1.1(KOMP)Vlcg/Lpar4tm1.1(KOMP)Vlcg
C57BL/6N-Lpar4tm1.1(KOMP)Vlcg/J 		decreased urine magnesium level J:211773
Lpar4tm1Sati/Y
involves: C57BL/6 		abnormal embryo development J:167262
abnormal fluid regulation J:167262
abnormal pericyte morphology J:167262
abnormal skin vasculature morphology J:167262
absent mandible J:167262
decreased embryo size J:167262
decreased fetal size J:167262
hemopericardium J:167262
hemorrhage J:167262
internal hemorrhage J:167262
lung hemorrhage J:167262
lymphangiectasis J:167262
omphalocele J:167262
pericardial effusion J:167262
prenatal lethality, incomplete penetrance J:167262
preweaning lethality, incomplete penetrance J:167262
skin edema J:167262
vascular smooth muscle hypoplasia J:167262
Lpar4tm1Sati/Lpar4tm1Sati
involves: C57BL/6 		abnormal embryo development J:167262
abnormal fluid regulation J:167262
abnormal pericyte morphology J:167262
abnormal skin vasculature morphology J:167262
absent mandible J:167262
decreased embryo size J:167262
decreased fetal size J:167262
hemopericardium J:167262
hemorrhage J:167262
internal hemorrhage J:167262
lung hemorrhage J:167262
lymphangiectasis J:167262
omphalocele J:167262
pericardial effusion J:167262
prenatal lethality, incomplete penetrance J:167262
preweaning lethality, incomplete penetrance J:167262
skin edema J:167262
vascular smooth muscle hypoplasia J:167262
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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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory