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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Pcgf2
polycomb group ring finger 2
MGI:99161
44 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background		 Annotated Term Reference
Mtf2tm1.1Hko/Mtf2tm1.1Hko
Pcgf2tm1Hko/Pcgf2tm1Hko
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 		abnormal occipital bone morphology J:170279
abnormal supraoccipital bone morphology J:170279
cervical vertebral transformation J:170279
increased rib number J:170279
lumbar vertebral transformation J:170279
perinatal lethality, complete penetrance J:170279
scapular bone foramen J:170279
thoracic vertebral transformation J:170279
vertebral transformation J:170279
Pcgf2tm1Hko/Pcgf2+
Bmi1tm1Brn/Bmi1tm1Brn
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 		abnormal axial skeleton morphology J:68216
abnormal cervical atlas morphology J:68216
abnormal craniofacial bone morphology J:68216
abnormal rib joint morphology J:68216
abnormal scapula morphology J:68216
abnormal sternum ossification J:68216
acromion hypoplasia J:68216
cervical vertebral transformation J:68216
cleft secondary palate J:68216
scapular bone foramen J:68216
split exoccipital bone J:68216
Pcgf2tm1Hko/Pcgf2+
Sf3b1tm1Hko/Sf3b1+
involves: C57BL/6 		abnormal sternocostal joint morphology J:96358
abnormal sternum ossification J:96358
cervical vertebral transformation J:96358
lumbar vertebral transformation J:96358
thoracic vertebral transformation J:96358
vertebral transformation J:96358
Pcgf2tm1Hko/Pcgf2tm1Hko
Bmi1tm1Brn/Bmi1+
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 		abnormal axial skeleton morphology J:68216
abnormal cervical atlas morphology J:68216
abnormal craniofacial bone morphology J:68216
abnormal rib joint morphology J:68216
abnormal scapula morphology J:68216
abnormal sternum ossification J:68216
acromion hypoplasia J:68216
cervical vertebral transformation J:68216
cleft secondary palate J:68216
scapular bone foramen J:68216
split exoccipital bone J:68216
Pcgf2tm1Hko/Pcgf2tm1Hko
Bmi1tm1Brn/Bmi1tm1Brn
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 		abnormal brain morphology J:68216
abnormal cervical atlas morphology J:68216
abnormal dorsal aorta morphology J:68216
abnormal first pharyngeal arch morphology J:68216
abnormal neural tube morphology J:68216
abnormal notochord morphology J:68216
abnormal optic eminence morphology J:68216
abnormal second pharyngeal arch morphology J:68216
abnormal somatic mesoderm morphology J:68216
abnormal somite development J:68216
abnormal tail bud morphology J:68216
cervical vertebral transformation J:68216
embryonic growth arrest J:68216
embryonic lethality during organogenesis, complete penetrance J:68216
hindbrain hypoplasia J:68216
increased neural tube apoptosis J:68216
small notochord J:68216
split notochord J:68216
Pcgf2tm1Hko/Pcgf2tm1Hko
Phc2tm1Hko/Phc2tm1Hko
involves: 129S1/Sv * 129X1/SvJ 		abnormal skeleton morphology J:170279
prenatal lethality, complete penetrance J:170279
Pcgf2tm1Hko/Pcgf2tm1Hko
Phc2tm1Hko/Phc2tm1Hko
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 		abnormal basioccipital bone morphology J:100027
abnormal bone ossification J:100027
abnormal hyoid bone morphology J:100027
abnormal occipital bone morphology J:100027
abnormal skeleton morphology J:100027
abnormal thoracic cage morphology J:100027
perinatal lethality, complete penetrance J:100027
Pcgf2tm1Hko/Pcgf2tm1Hko
Rnf2tm1Hko/Rnf2tm1Hko
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 		abnormal vertebrae morphology J:79851
asymmetric sternocostal joints J:79851
normal skeleton phenotype J:79851
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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Send questions and comments to User Support. 		last database update
11/19/2024
MGI 6.24 		The Jackson Laboratory