53 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Mmp14tm1Hbh/Mmp14+ Mmp16tm1Khol/Mmp16+ involves: 129P2/OlaHsd * 129S6/SvEvTac	abnormal chondrocyte morphology	J:130212
	decreased cranium length	J:130212
	short humerus	J:130212
Mmp14tm1Hbh/Mmp14+ Mmp16tm1Khol/Mmp16tm1Khol involves: 129P2/OlaHsd * 129S6/SvEvTac	abnormal chondrocyte morphology	J:130212
	abnormal compact bone morphology	J:130212
	decreased bone ossification	J:130212
	decreased cranium length	J:130212
	frontal bone hypoplasia	J:130212
	nasal bone hypoplasia	J:130212
	parietal bone hypoplasia	J:130212
	postnatal lethality, incomplete penetrance	J:130212
	short femur	J:130212
	short humerus	J:130212
	short snout	J:130212
	thin neurocranium	J:130212
Mmp14tm1Hbh/Mmp14tm1.1Khol Mmp15tm1Kohl/Mmp15tm1Kohl Tg(CAG-cre/Esr1*)5Amc/0 involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * CBA	abnormal placental labyrinth vasculature morphology	J:167396
	absent placental labyrinth	J:167396
	normal endocrine/exocrine gland phenotype	J:167396
Mmp14tm1Hbh/Mmp14tm1Hbh Mmp15tm1Kohl/Mmp15tm1Kohl involves: 129P2/OlaHsd * 129S6/SvEvTac	abnormal placenta labyrinth morphology	J:167396
	abnormal placental labyrinth vasculature morphology	J:167396
	decreased embryo size	J:167396
	dilated vasculature	J:167396
	embryonic growth retardation	J:167396
	embryonic lethality during organogenesis, complete penetrance	J:167396
	enlarged pericardium	J:167396
Mmp14tm1Hbh/Mmp14tm1Hbh Mmp16tm1Khol/Mmp16+ involves: 129P2/OlaHsd * 129S6/SvEvTac	abnormal cartilage morphology	J:130212
	abnormal chondrocyte morphology	J:130212
	abnormal compact bone morphology	J:130212
	abnormal long bone epiphyseal plate proliferative zone	J:130212
	abnormal long bone hypertrophic chondrocyte zone	J:130212
	abnormal long bone morphology	J:130212
	decreased bone ossification	J:130212
	frontal bone hypoplasia	J:130212
	nasal bone hypoplasia	J:130212
	parietal bone hypoplasia	J:130212
	postnatal lethality, complete penetrance	J:130212
	short femur	J:130212
	short humerus	J:130212
	thin neurocranium	J:130212
Mmp14tm1Hbh/Mmp14tm1Hbh Mmp16tm1Khol/Mmp16tm1Khol involves: 129P2/OlaHsd * 129S6/SvEvTac	abnormal cartilage morphology	J:130212
	abnormal chondrocyte morphology	J:130212
	abnormal compact bone morphology	J:130212
	abnormal cranium morphology	J:130212
	abnormal long bone epiphyseal plate proliferative zone	J:130212
	abnormal long bone hypertrophic chondrocyte zone	J:130212
	abnormal long bone morphology	J:130212
	abnormal mandible morphology	J:130212
	abnormal Meckel's cartilage morphology	J:130212
	abnormal midface morphology	J:130212
	abnormal parietal bone morphology	J:130212
	abnormal skeleton morphology	J:130212
	abnormal vomer bone morphology	J:130212
	absent bone trabeculae	J:130212
	absent palatine bone	J:130212
	cleft secondary palate	J:130212
	decreased body size	J:130212
	decreased bone ossification	J:130212
	domed cranium	J:130212
	frontal bone hypoplasia	J:130212
	maxilla hypoplasia	J:130212
	nasal bone hypoplasia	J:130212
	neonatal lethality, complete penetrance	J:130212
	palatal shelf hypoplasia	J:130212
	palatal shelves fail to meet at midline	J:130212
	parietal bone hypoplasia	J:130212
	pterygoid bone hypoplasia	J:130212
	short femur	J:130212
	short humerus	J:130212
	short limbs	J:130212
	short snout	J:130212
	thin neurocranium	J:130212
	vomer bone hypoplasia	J:130212
Mmp14tm1Noda/Mmp14+ Mmp2tm1Ito/Mmp2tm1Ito Not Specified	decreased body weight	J:91198
Mmp14tm1Noda/Mmp14tm1Noda Mmp2tm1Ito/Mmp2tm1Ito Not Specified	abnormal blood vessel morphology	J:91198
	abnormal bone ossification	J:91198
	abnormal skeletal muscle morphology	J:91198
	abnormal skeleton morphology	J:91198
	cyanosis	J:91198
	decreased birth weight	J:91198
	delayed muscle development	J:91198
	neonatal lethality, complete penetrance	J:91198
	thin diaphragm muscle	J:91198