48 phenotypes from 5 alleles in 7 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Evc2em1(IMPC)Mbp/Evc2em1(IMPC)Mbp C57BL/6N-Evc2em1(IMPC)Mbp/MbpMmucd	abnormal cecum morphology	J:211773
	abnormal gallbladder morphology	J:211773
	abnormal heart morphology	J:211773
	abnormal retina morphology	J:211773
	abnormal skin morphology	J:211773
	abnormal spleen morphology	J:211773
	abnormal uterus morphology	J:211773
	absent teeth	J:211773
	decreased blood urea nitrogen level	J:211773
	decreased body length	J:211773
	decreased circulating total protein level	J:211773
	decreased grip strength	J:211773
	decreased prepulse inhibition	J:211773
	enlarged heart	J:211773
	hydrometra	J:211773
	small spleen	J:211773
Evc2tm1.1Mis/Evc2tm1.1Mis involves: 129X1/SvJ * C57BL/6	decreased body length	J:226455
	decreased body weight	J:226455
	decreased bone mineral content	J:226455
	decreased trabecular bone volume	J:226455
	disproportionate dwarf	J:226455
	microcephaly	J:226455
	preweaning lethality, incomplete penetrance	J:226455
	short femur	J:226455
	short fibula	J:226455
	short humerus	J:226455
	short limbs	J:226455
	short radius	J:226455
	short tibia	J:226455
	short ulna	J:226455
	slow postnatal weight gain	J:226455
	small cranium	J:226455
	small upper incisors	J:226455
Evc2tm1.1Vlrp/Evc2tm1.1Vlrp involves: 129 * C57BL/6J	abnormal basicranium morphology	J:188176
	abnormal chondrocyte physiology	J:188176
	abnormal long bone epiphyseal plate morphology	J:188176
	abnormal long bone epiphyseal plate proliferative zone	J:188176
	decreased width of hypertrophic chondrocyte zone	J:188176
	impaired osteoblast differentiation	J:188176
	perinatal lethality, complete penetrance	J:188176
	short femur	J:188176
	short limbs	J:188176
	short radius	J:188176
	short ribs	J:188176
	short tibia	J:188176
Evc2tm2.1Mis/Evc2tm2.1Mis Edil3Tg(Sox2-cre)1Amc/Edil3+ involves: 129X1/SvJ * C57BL/6 * CBA	disproportionate dwarf	J:226455
Evc2tm2.1Mis/Evc2tm2.1Mis Tg(Col2a1-cre/ERT)KA3Smac/0 involves: 129X1/SvJ * FVB/N	disproportionate dwarf	J:226455
	short femur	J:226455
	short fibula	J:226455
	short humerus	J:226455
	short radius	J:226455
	short tibia	J:226455
	short ulna	J:226455
Evc2tm2.1Mis/Evc2tm2.1Mis Tg(Mpz-cre)94Imeg/0 involves: 129X1/SvJ	abnormal ameloblast morphology	J:226455
	abnormal tooth development	J:226455
	normal mortality/aging	J:226455
	short lower incisors	J:226455
	short upper incisors	J:226455
Evc2tm2.1Mis/Evc2tm2.1Mis Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0 involves: 129X1/SvJ * CD-1	normal growth/size/body region phenotype	J:226455
	normal skeleton phenotype	J:226455
Evc2tm2Mis/Evc2tm2Mis involves: 129X1/SvJ	no abnormal phenotype detected	J:226455