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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Peg3
paternally expressed 3
MGI:104748
16 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Peg3tm1.1Jkim/Peg3+
involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J
abnormal imprinting J:184471
normal cellular phenotype J:184471
decreased body weight J:184471
embryonic lethality during organogenesis, incomplete penetrance J:184471
increased body weight J:184471
Peg3tm1a(EUCOMM)Hmgu/Peg3+
involves: C57BL/6N
absent gastric milk in neonates J:209833
decreased body weight J:209833
decreased oocyte number J:209833
postnatal growth retardation J:209833
postnatal lethality, incomplete penetrance J:209833
small testis J:209833
Peg3tm1Masu/Peg3+
involves: 129S1/Sv * 129X1/SvJ
abnormal hypothalamus morphology J:54324
abnormal pup retrieval J:54324
absent maternal crouching J:54324
decreased body weight J:54324
normal endocrine/exocrine gland phenotype J:54324
maternal imprinting J:54324
normal nervous system phenotype J:54324

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
04/23/2024
MGI 6.23
The Jackson Laboratory