Peg3 Phenotype Annotations

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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

Allelic Composition Genetic Background	Annotated Term	Reference
Peg3^tm1.1Jkim/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
Peg3^{tm1a(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
Peg3^tm1Masu/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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