70 phenotypes from 4 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fuzb2b1273Clo/Fuzb2b1273Clo C57BL/6J-Fuzb2b1273Clo	abnormal liver morphology	J:175213
	anophthalmia	J:175213
	atrioventricular septal defect	J:175213
	diaphragmatic hernia	J:175213
	dual inferior vena cava	J:175213
	multiple major aortopulmonary collateral arteries	J:175213
	polydactyly	J:175213
	pulmonary hypoplasia	J:175213
	pulmonary valve atresia	J:175213
	right aortic arch	J:175213
	tracheoesophageal fistula	J:175213
Fuzem1(IMPC)Mbp/Fuzem1(IMPC)Mbp C57BL/6N-Fuzem1(IMPC)Mbp/MbpMmucd	abnormal craniofacial morphology	J:211773
	abnormal facial morphology	J:211773
	abnormal heart looping	J:211773
	abnormal heart morphology	J:211773
	abnormal limb morphology	J:211773
	abnormal neural tube closure	J:211773
	abnormal neural tube morphology	J:211773
	abnormal optic vesicle formation	J:211773
	abnormal tail morphology	J:211773
	anophthalmia	J:211773
	cleft palate	J:211773
	edema	J:211773
	facial cleft	J:211773
	hemorrhage	J:211773
	polydactyly	J:211773
	preweaning lethality, complete penetrance	J:211773
	syndactyly	J:211773
FuzGt(AN0439)Wtsi/FuzGt(AN0439)Wtsi involves: 129P2/OlaHsd * C3H	abnormal apical ectodermal ridge morphology	J:154370
	abnormal developmental patterning	J:154370
	abnormal midbrain morphology	J:154370
	abnormal motor neuron morphology	J:154370
	abnormal neural tube closure	J:154370
	abnormal primary cilium morphology	J:154370
	abnormal spinal cord morphology	J:154370
	abnormal ventral interneuron 3 morphology	J:154370
	absent eye pigmentation	J:154370
	edema	J:154370
	lethality throughout fetal growth and development, complete penetrance	J:154370
	microphthalmia	J:154370
	pericardial edema	J:154370
	polydactyly	J:154370
	small floor plate	J:154370
FuzGt(OSTGST001398)Lex/FuzGt(OSTGST001398)Lex involves: 129S5/SvEvBrd * C57BL/6	abnormal brain development	J:177881
	abnormal cochlea morphology	J:177881
	abnormal craniofacial morphology	J:177881
	abnormal diencephalon morphology	J:177881
	abnormal head mesenchyme morphology	J:177881
	abnormal mandible morphology	J:177881
	abnormal Meckel's cartilage morphology	J:177881
	abnormal palate development	J:177881
	abnormal pituitary diverticulum morphology	J:177881
	abnormal striatum morphology	J:177881
	abnormal tongue morphology	J:177881
	abnormal tooth development	J:177881
	absent choroid plexus	J:177881
	absent incisors	J:177881
	anophthalmia	J:177881
	cleft secondary palate	J:177881
	delayed bone ossification	J:177881
	delayed intramembranous bone ossification	J:177881
	delayed palatal shelf elevation	J:177881
	mandible hypoplasia	J:177881
	maxilla hypoplasia	J:177881
	Meckel's cartilage hyperplasia	J:177881
	neonatal lethality, complete penetrance	J:177881
	tongue ankylosis	J:177881
FuzGt(OSTGST001398)Lex/FuzGt(OSTGST001398)Lex involves: 129S5/SvEvBrd * C57BL/6N	abnormal cardiac outflow tract development	J:158243
	abnormal craniofacial morphology	J:158243
	abnormal eye morphology	J:158243
	abnormal long bone morphology	J:158243
	abnormal Meckel's cartilage morphology	J:158243
	abnormal rib morphology	J:158243
	abnormal sternum morphology	J:158243
	abnormal truncus arteriosus septation	J:158243
	anophthalmia	J:158243
	dilated brain ventricle	J:158243
	encephalomeningocele	J:158243
	exencephaly	J:158243
	persistent truncus arteriosus	J:158243
	polydactyly	J:158243
	pulmonary hypoplasia	J:158243