73 phenotypes from 7 alleles in 10 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ccn2tm1.1(folA/cre)Hze/Ccn2+ involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * C57BL/6NCr	no abnormal phenotype detected	J:227758
Ccn2tm1.1Alea/Ccn2tm1.1Alea Tg(Col1a2-cre/ERT,-ALPP)7Cpd/0 involves: 129S2/SvPas * C57BL/6 * DBA/2	abnormal skin physiology	J:171300
	decreased physiological sensitivity to xenobiotic	J:171300
Ccn2tm1.1Vlcg/Ccn2tm1.1Vlcg involves: 129S6/SvEvTac * C57BL/6NTac	no abnormal phenotype detected	J:200671
Ccn2tm1.1Vlcg/Ccn2tm1.1Vlcg Tg(Prrx1-cre)1Cjt/0 involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac * SJL/J	abnormal trabecular bone morphology	J:163027
	decreased bone mineral density	J:163027
Ccn2tm1Kml/Ccn2tm1Kml involves: 129X1/SvJ * BALB/cJ	abnormal appendicular skeleton morphology	J:83260
	abnormal axial skeleton morphology	J:83260
	abnormal cartilage development	J:83260
	abnormal cartilage morphology	J:83260
	abnormal cervical atlas morphology	J:83260
	abnormal chondrocyte physiology	J:83260
	abnormal long bone hypertrophic chondrocyte zone	J:83260
	abnormal long bone morphology	J:83260
	abnormal lung development	J:130165
	abnormal Meckel's cartilage morphology	J:83260
	abnormal nasal cartilage morphology	J:83260
	abnormal pulmonary alveolus morphology	J:130165
	abnormal respiratory conducting tube morphology	J:130165
	abnormal rib morphology	J:83260
	abnormal sternebra morphology	J:83260
	abnormal thoracic cage morphology	J:83260
	abnormal type II pneumocyte morphology	J:130165
	abnormal vertebrae morphology	J:83260
	abnormal vertebral column morphology	J:83260
	absent ethmoid bone	J:83260
	bowed fibula	J:83260
	bowed radius	J:83260
	bowed tibia	J:83260
	bowed ulna	J:83260
	normal cardiovascular system phenotype	J:83260
	chondrodystrophy	J:83260
	cleft secondary palate	J:83260
	decreased angiogenesis	J:83260
	decreased bone mineral density of femur	J:83260
	decreased lung weight	J:130165
	decreased mesenchymal cell proliferation involved in lung development	J:130165
	decreased trabecular bone thickness	J:83260
	delayed endochondral bone ossification	J:83260
	disorganized long bone epiphyseal plate	J:83260
	domed cranium	J:83260
	failure of palatal shelf elevation	J:83260
	increased long bone epiphyseal plate size	J:83260
	increased width of hypertrophic chondrocyte zone	J:83260
	neonatal lethality, complete penetrance	J:83260
	pectus excavatum	J:83260
	pulmonary hypoplasia	J:130165
	respiratory failure	J:83260
	short mandible	J:83260
	short sternum	J:83260
	small alveolar lamellar bodies	J:130165
	small lung	J:130165
	small lung saccule	J:130165
	small thoracic cavity	J:83260
Ccn2tm1Mae/Ccn2tm1Mae 129S6/SvEvTac-Ccn2tm1Mae	neonatal lethality, complete penetrance	J:165111
Ccn2tm1Mae/Ccn2tm2Mae involves: 129S6/SvEvTac	no abnormal phenotype detected	J:165111
Ccn2tm1Mga/Ccn2+ involves: 129S6/SvEvTac * C57BL/6NTac	abnormal trabecular bone morphology	J:163027
	decreased bone mineral density	J:163027
Ccn2tm1Mga/Ccn2tm1.1Vlcg Tg(BGLAP-cre)1Clem/0 involves: 129S6/SvEvTac * C57BL/6NTac * FVB/NJ	abnormal trabecular bone morphology	J:163027
	decreased bone mineral density	J:163027
Ccn2tm1Mga/Ccn2tm1Mga involves: 129S6/SvEvTac * C57BL/6NTac	abnormal angiogenesis	J:145696
	abnormal bone ossification	J:145696
	abnormal sternum morphology	J:145696
	abnormal vertebrae morphology	J:145696
	chondrodystrophy	J:145696
	neonatal lethality, complete penetrance	J:145696
	respiratory failure	J:145696
Ccn2tm2Mae/Ccn2+ Tg(EIIa-cre)C5379Lmgd/? involves: 129S6/SvEvTac	abnormal bone structure	J:165111
	abnormal facial morphology	J:165111
	abnormal pharyngeal arch development	J:165111
	abnormal vasculogenesis	J:165111
	decreased bone mineral content	J:165111
	decreased lean body mass	J:165111
	embryonic growth retardation	J:165111
	embryonic lethality during organogenesis, complete penetrance	J:165111
	kinked tail	J:165111
	short tail	J:165111
	small ears	J:165111
Ccn2tm2Mae/Ccn2+ Tg(EIIa-cre)C5379Lmgd/? involves: 129S6/SvEvTac * C57BL/6 * FVB/N	abnormal bone structure	J:165111
	abnormal eye development	J:165111
	abnormal vasculogenesis	J:165111
	decreased bone mineral content	J:165111
	decreased embryo size	J:165111
	decreased lean body mass	J:165111
	embryonic growth retardation	J:165111
	embryonic lethality during organogenesis, complete penetrance	J:165111
	facial cleft	J:165111
	kinked tail	J:165111
	lateral facial cleft	J:165111
	midline facial cleft	J:165111
	short face	J:165111
	short tail	J:165111
	small ears	J:165111
Ccn2tm2Mae/Ccn2+ Tg(CAG-cre/Esr1*)5Amc/? involves: 129S6/SvEvTac * C57BL/6 * CBA	no abnormal phenotype detected	J:165111