Pcgf6 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Pcgf6
polycomb group ring finger 6
MGI:1918291

18 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Pcgf6^tm1.2Hko/Pcgf6^tm1.2Hko involves: 129 * C57BL/6	abnormal arcus anterior morphology	J:258919
	abnormal placenta development	J:258919
	abnormal placenta labyrinth morphology	J:258919
	abnormal pluripotent precursor cell morphology	J:258919
	abnormal preimplantation embryo development	J:258919
	abnormal rostral-caudal axis patterning	J:258919
	abnormal sternocostal joint morphology	J:258919
	cervical vertebral transformation	J:258919
	decreased nucleated erythrocyte cell number	J:258919
	decreased spongiotrophoblast cell number	J:258919
	decreased trophoblast giant cell number	J:258919
	embryonic growth retardation	J:258919
	increased rib number	J:258919
	placental labyrinth hypoplasia	J:258919
	prenatal lethality, incomplete penetrance	J:258919
	rib fusion	J:258919
	small placenta	J:258919
	thoracic vertebral transformation	J:258919

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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