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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Phc2
polyhomeotic 2
MGI:1860454
29 phenotypes from multigenic genotypes
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Mtf2tm1.1Hko/Mtf2+
Phc2tm1Hko/Phc2tm1Hko
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal skeleton morphology J:170279
prenatal lethality, complete penetrance J:170279
Mtf2tm1.1Hko/Mtf2tm1.1Hko
Phc2tm1Hko/Phc2tm1Hko
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal supraoccipital bone morphology J:170279
cervical vertebral transformation J:170279
early cellular replicative senescence J:170279
lumbar vertebral transformation J:170279
prenatal lethality, complete penetrance J:170279
thoracic vertebral transformation J:170279
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
Phc1tm1Os/Phc1+
Phc2tm1Hko/Phc2+
involves: 129/Sv * C57BL/6
abnormal axial skeleton morphology J:100027
Phc1tm1Os/Phc1+
Phc2tm1Hko/Phc2tm1Hko
involves: 129/Sv * C57BL/6
abnormal cervical vertebrae morphology J:100027
abnormal occipital bone morphology J:100027
abnormal skeleton morphology J:100027
abnormal sternocostal joint morphology J:100027
cleft secondary palate J:100027
perinatal lethality, complete penetrance J:100027
scapular bone foramen J:100027
Phc1tm1Os/Phc1tm1Os
Phc2tm1Hko/Phc2+
involves: 129/Sv * C57BL/6
abnormal cervical vertebrae morphology J:100027
abnormal exoccipital bone morphology J:100027
abnormal skeleton morphology J:100027
abnormal sternocostal joint morphology J:100027
abnormal tympanic ring morphology J:100027
absent presphenoid bone J:100027
cleft secondary palate J:100027
perinatal lethality, complete penetrance J:100027
scapular bone foramen J:100027
Phc1tm1Os/Phc1tm1Os
Phc2tm1Hko/Phc2tm1Hko
involves: 129/Sv * C57BL/6
abnormal first pharyngeal arch morphology J:100027
abnormal second pharyngeal arch morphology J:100027
embryonic growth retardation J:100027
embryonic lethality during organogenesis, complete penetrance J:100027
incomplete somite formation J:100027
small tail bud J:100027
Phc2tm1Hko/Phc2+
Scmh1tm1Hko/Scmh1tm1Hko
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal spermatogenesis J:119909
Phc2tm1Hko/Phc2tm1Hko
Scmh1tm1Hko/Scmh1tm1Hko
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
normal reproductive system phenotype J:119909

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
04/06/2021
MGI 6.16
The Jackson Laboratory