Phc2 Phenotype Annotations - Multigenic Genotypes

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Phc2
polyhomeotic 2
MGI:1860454

29 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Mtf2^tm1.1Hko/Mtf2⁺ Phc2^tm1Hko/Phc2^tm1Hko involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal skeleton morphology	J:170279
	prenatal lethality, complete penetrance	J:170279
Mtf2^tm1.1Hko/Mtf2^tm1.1Hko Phc2^tm1Hko/Phc2^tm1Hko 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
Pcgf2^tm1Hko/Pcgf2^tm1Hko Phc2^tm1Hko/Phc2^tm1Hko involves: 129S1/Sv * 129X1/SvJ	abnormal skeleton morphology	J:170279
	prenatal lethality, complete penetrance	J:170279
Pcgf2^tm1Hko/Pcgf2^tm1Hko Phc2^tm1Hko/Phc2^tm1Hko 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
Phc1^tm1Os/Phc1⁺ Phc2^tm1Hko/Phc2⁺ involves: 129/Sv * C57BL/6	abnormal axial skeleton morphology	J:100027
Phc1^tm1Os/Phc1⁺ Phc2^tm1Hko/Phc2^tm1Hko 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
Phc1^tm1Os/Phc1^tm1Os Phc2^tm1Hko/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
Phc1^tm1Os/Phc1^tm1Os Phc2^tm1Hko/Phc2^tm1Hko 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
Phc2^tm1Hko/Phc2⁺ Scmh1^tm1Hko/Scmh1^tm1Hko involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal spermatogenesis	J:119909
Phc2^tm1Hko/Phc2^tm1Hko Scmh1^tm1Hko/Scmh1^tm1Hko 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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