30 phenotypes from 4 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Pnntm1.1(KOMP)Vlcg/Pnntm1.1(KOMP)Vlcg C57BL/6N-Pnntm1.1(KOMP)Vlcg/Ucd	embryonic lethality prior to organogenesis	J:211773
	embryonic lethality prior to tooth bud stage	J:211773
	preweaning lethality, complete penetrance	J:211773
Pnntm1.1Sps/Pnntm1.2Sps Tg(Pax6-cre,GFP)1Pgr/0 involves: 129S4/SvJae * FVB	abnormal cornea morphology	J:160411
	abnormal corneal stroma morphology	J:160411
	abnormal lens morphology	J:160411
	irregularly shaped pupil	J:160411
	microphthalmia	J:160411
	normal vision/eye phenotype	J:160411
Pnntm1.2Sps/Pnntm1.2Sps involves: 129S4/SvJae * C57BL/6	embryonic lethality before implantation, complete penetrance	J:123288
Pnntm1Sps/Pnntm1.2Sps involves: 129S4/SvJae * C57BL/6	embryonic lethality during organogenesis, complete penetrance	J:123288
	failure of primitive streak formation	J:123288
	failure to gastrulate	J:123288
Pnntm1Sps/Pnntm1Sps involves: 129S4/SvJae * C57BL/6	abnormal cardiac outflow tract development	J:123288
	abnormal dermal layer morphology	J:123288
	abnormal rib morphology	J:123288
	cleft palate	J:123288
	decreased brown adipose tissue amount	J:123288
	decreased hair follicle number	J:123288
	double outlet right ventricle	J:123288
	edema	J:123288
	embryonic growth retardation	J:123288
	normal integument phenotype	J:123288
	lumbar vertebral transformation	J:123288
	perinatal lethality, complete penetrance	J:123288
	persistent truncus arteriosus	J:123288
	rib fusion	J:123288
	thin dermal layer	J:123288
	transposition of great arteries	J:123288
	ventricular septal defect	J:123288