About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
04/30/2024
MGI 6.23 		The Jackson Laboratory