57 phenotypes from 5 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
H2az2Tg(Wnt1-cre)11Rth/H2az2+ Memo1tm1c(EUCOMM)Wtsi/Memo1tm1c(EUCOMM)Wtsi involves: C57BL/6 * CBA/J * SJL	abnormal craniofacial bone morphology	J:233609
	abnormal endochondral bone ossification	J:233609
	abnormal nasal bridge morphology	J:233609
	absent gastric milk in neonates	J:233609
	cleft palate	J:233609
	domed cranium	J:233609
	maxillary shelf hypoplasia	J:233609
	palatine bone horizontal plate hypoplasia	J:233609
	premaxilla hypoplasia	J:233609
	presphenoid bone hypoplasia	J:233609
	preweaning lethality, complete penetrance	J:233609
	small basisphenoid bone	J:233609
	wide coronal suture	J:233609
	wide metopic suture	J:233609
Memo1m1Will/Memo1m1Will involves: 129S1/SvImJ * C57BL/6J	abnormal bone ossification	J:233609
	abnormal cranial cartilage development	J:233609
	abnormal craniofacial bone morphology	J:233609
	abnormal cranium morphology	J:233609
	abnormal endochondral bone ossification	J:233609
	abnormal nasal bridge morphology	J:233609
	abnormal neurocranium morphology	J:233609
	abnormal otic capsule morphology	J:233609
	abnormal vasculogenesis	J:233609
	absent gastric milk in neonates	J:233609
	absent maxillary shelf	J:233609
	absent palatine bone horizontal plate	J:233609
	basioccipital bone hypoplasia	J:233609
	basisphenoid bone hypoplasia	J:233609
	cleft palate	J:233609
	decreased angiogenesis	J:233609
	domed cranium	J:233609
	embryonic lethality during organogenesis	J:233609
	failure of endochondral bone ossification	J:233609
	failure of palatal shelf elevation	J:233609
	generalized edema	J:233609
	hemorrhage	J:233609
	maxilla hypoplasia	J:233609
	palate bone hypoplasia	J:233609
	premaxilla hypoplasia	J:233609
	presphenoid bone hypoplasia	J:233609
	preweaning lethality, complete penetrance	J:233609
Memo1tm1.1Neh/Memo1tm1.1Neh Tg(CAG-cre/Esr1*)1Lbe/0 involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	abnormal coat/hair pigmentation	J:206626
	abnormal reflex	J:206626
	abnormal sex gland morphology	J:206626
	alopecia	J:206626
	azoospermia	J:206626
	decreased body size	J:206626
	decreased body weight	J:206626
	decreased subcutaneous adipose tissue amount	J:206626
	decreased white adipose tissue amount	J:206626
	normal homeostasis/metabolism phenotype	J:206626
	improved glucose tolerance	J:206626
	increased circulating calcium level	J:206626
	increased circulating parathyroid hormone level	J:206626
	increased insulin sensitivity	J:206626
	increased vitamin D level	J:206626
	kyphosis	J:206626
	premature death	J:206626
	weight loss	J:206626
Memo1tm1a(EUCOMM)Wtsi/Memo1+ C57BL/6N-Memo1tm1a(EUCOMM)Wtsi/Bay	trunk curl	J:211773
Memo1tm1a(EUCOMM)Wtsi/Memo1tm1a(EUCOMM)Wtsi C57BL/6N-Memo1tm1a(EUCOMM)Wtsi/Bay	preweaning lethality, complete penetrance	J:211773
Memo1tm1b(EUCOMM)Wtsi/Memo1+ C57BL/6N-Memo1tm1b(EUCOMM)Wtsi/Bay	thick ventricular wall	J:211773
	unresponsive to tactile stimuli	J:211773
Memo1tm1b(EUCOMM)Wtsi/Memo1tm1b(EUCOMM)Wtsi C57BL/6N-Memo1tm1b(EUCOMM)Wtsi/Bay	abnormal embryo size	J:211773
	abnormal pericardium morphology	J:211773
	edema	J:211773
	hemorrhage	J:211773
	preweaning lethality, complete penetrance	J:211773
	unresponsive to tactile stimuli	J:211773
Memo1tm1b(EUCOMM)Wtsi/Memo1tm1b(EUCOMM)Wtsi involves: Black Swiss * C57BL/6 * FVB/N	abnormal nasal bridge morphology	J:233609
	cleft secondary palate	J:233609
	domed cranium	J:233609
	preweaning lethality, complete penetrance	J:233609