Pcgf1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Pcgf1
polycomb group ring finger 1
MGI:1917087

13 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Pcgf1^{tm1.1(KOMP)Vlcg}/Pcgf1⁺ C57BL/6N-Pcgf1^{tm1.1(KOMP)Vlcg}/J	hyperactivity	J:211773
	increased fasting circulating glucose level	J:211773
Pcgf1^{tm1.1(KOMP)Vlcg}/Pcgf1^{tm1.1(KOMP)Vlcg} C57BL/6N-Pcgf1^{tm1.1(KOMP)Vlcg}/J	abnormal embryo size	J:211773
	abnormal embryo turning	J:211773
	abnormal forebrain development	J:211773
	abnormal heart looping	J:211773
	abnormal heart morphology	J:211773
	abnormal midbrain development	J:211773
	abnormal neural tube closure	J:211773
	abnormal pharyngeal arch morphology	J:211773
	embryonic growth retardation	J:211773
	embryonic lethality prior to tooth bud stage	J:211773
	preweaning lethality, complete penetrance	J:211773

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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