29 phenotypes from 3 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Pcgf2tm1b(KOMP)Mbp/Pcgf2+ C57BL/6N-Pcgf2tm1b(KOMP)Mbp/Tcp	abnormal lumbar vertebrae morphology	J:211773
	abnormal spleen morphology	J:211773
	abnormal testis morphology	J:211773
	increased bone mineral content	J:211773
	small spleen	J:211773
	small testis	J:211773
Pcgf2tm1b(KOMP)Mbp/Pcgf2tm1b(KOMP)Mbp C57BL/6N-Pcgf2tm1b(KOMP)Mbp/Tcp	preweaning lethality, complete penetrance	J:211773
Pcgf2tm1Hko/Pcgf2+ involves: C57BL/6	cervical vertebral transformation	J:96358
	lumbar vertebral transformation	J:96358
	thoracic vertebral transformation	J:96358
Pcgf2tm1Hko/Pcgf2tm1Hko involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal axial skeleton morphology	J:33159
	abnormal exoccipital bone morphology	J:33159
	abnormal occipital bone morphology	J:79851
	abnormal odontoid process morphology	J:33159
	abnormal rib morphology	J:33159, J:79851
	abnormal sternocostal joint morphology	J:33159
	abnormal sternum ossification	J:33159
	abnormal supraoccipital bone morphology	J:33159
	cervical vertebral transformation	J:33159
	lumbar vertebral transformation	J:33159
	perinatal lethality, incomplete penetrance	J:79851
	postnatal growth retardation	J:33159
	premature death	J:33159
	rib fusion	J:33159
	sacral vertebral transformation	J:33159
	thoracic vertebral transformation	J:33159
	vertebral transformation	J:33159
Pcgf2tm1Hko/Pcgf2tm1Hko involves: BALB/c * C57BL/6	abnormal T-helper 2 physiology	J:71268
	decreased lymphocyte cell number	J:71268
	decreased thymocyte number	J:71268
Pcgf2tm2.1Hko/Pcgf2tm2.1Hko involves: 129S1/Sv * 129X1/SvJ	normal reproductive system phenotype	J:204987
	normal skeleton phenotype	J:204987