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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
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Allelic Composition
Genetic Background
Annotated Term Reference
Pcgf6tm1.2Hko/Pcgf6tm1.2Hko
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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last database update
01/24/2023
MGI 6.22
The Jackson Laboratory