72 phenotypes from 6 alleles in 6 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ncor2em1(IMPC)Mbp/Ncor2+ C57BL/6N-Ncor2em1(IMPC)Mbp/MbpMmucd	abnormal blood vessel morphology	J:211773
	abnormal placenta morphology	J:211773
	abnormal retina morphology	J:211773
	embryonic growth retardation	J:211773
	persistence of hyaloid vascular system	J:211773
Ncor2em1(IMPC)Mbp/Ncor2em1(IMPC)Mbp C57BL/6N-Ncor2em1(IMPC)Mbp/MbpMmucd	abnormal blood vessel morphology	J:211773
	abnormal craniofacial morphology	J:211773
	abnormal placenta morphology	J:211773
	abnormal placenta vasculature	J:211773
	edema	J:211773
	preweaning lethality, complete penetrance	J:211773
Ncor2Gt(RRM275)Byg/Ncor2+ B6.129P2-Ncor2Gt(RRM275)Byg	abnormal cell differentiation	J:164558
	abnormal eating behavior	J:164558
	abnormal hormone level	J:164558
	abnormal white adipose tissue physiology	J:164558
	decreased carbon dioxide production	J:164558
	decreased circulating insulin level	J:164558
	decreased circulating leptin level	J:164558
	decreased energy expenditure	J:164558
	decreased oxygen consumption	J:164558
	decreased susceptibility to diet-induced hepatic steatosis	J:164558
	decreased white fat cell size	J:164558
	increased insulin sensitivity	J:164558
	increased susceptibility to diet-induced obesity	J:164558
	increased white adipose tissue amount	J:164558
	increased white fat cell number	J:164558
Ncor2Gt(RRM275)Byg/Ncor2Gt(RRM275)Byg B6.129P2-Ncor2Gt(RRM275)Byg	prenatal lethality, complete penetrance	J:164558
Ncor2tm1.1Ics/Ncor2tm1.1Ics involves: 129S2/SvPas * C57BL/6J	normal liver/biliary system phenotype	J:206152
Ncor2tm1Rev/Ncor2tm1Rev involves: 129/Sv * C57BL/6	abnormal bone marrow cavity morphology	J:202976
	abnormal bone marrow cell number	J:202976
	abnormal bone marrow morphology	J:202976
	abnormal cell differentiation	J:142665
	abnormal circulating enzyme level	J:202976
	abnormal circulating hormone level	J:202976
	abnormal gas homeostasis	J:142665
	abnormal gluconeogenesis	J:142665
	abnormal hematopoietic stem cell morphology	J:202976
	abnormal metabolism	J:142665
	abnormal physiological response to xenobiotic	J:142665
	abnormal skeleton physiology	J:202976
	abnormal spleen morphology	J:202976
	abnormal trabecular bone morphology	J:202976
	normal adipose tissue phenotype	J:142665
	decreased body temperature	J:142665
	decreased body weight	J:142665
	decreased bone strength	J:202976
	decreased carbon dioxide production	J:142665
	decreased compact bone thickness	J:202976
	decreased energy expenditure	J:142665
	decreased oxygen consumption	J:142665
	enlarged spleen	J:202976
	extramedullary hematopoiesis	J:202976
	hindlimb paresis	J:202976
	increased adiponectin level	J:142665
	increased bone trabecula number	J:202976
	increased circulating glucose level	J:142665
	increased epididymal fat pad weight	J:142665
	increased erythroid progenitor cell number	J:202976
	increased megakaryocyte cell number	J:202976
	increased osteoclast cell number	J:202976
	increased percent body fat/body weight	J:142665
	increased trabecular bone volume	J:202976
	insulin resistance	J:142665
	myelofibrosis	J:202976
	normal nervous system phenotype	J:142665
	osteosclerosis	J:202976
	thin ventricular wall	J:142665
Ncor2tm1Rsd/Ncor2tm1Rsd involves: 129S1/Sv * 129X1/SvJ	abnormal heart development	J:127720
	abnormal neuronal precursor proliferation	J:127720
	abnormal telencephalon morphology	J:127720
	lethality throughout fetal growth and development, complete penetrance	J:127720
	thin ventricular wall	J:132982
	ventricular septal defect	J:132982
Ncor2tm1Rsd/Ncor2tm1Rsd Tg(Myh6-Ncor2)1Kjep/? involves: 129/Sv * BALB/c * C57BL/6	abnormal cerebral cortex morphology	J:127720
	abnormal telencephalon development	J:127720
	cleft secondary palate	J:127720
	normal mortality/aging	J:127720
	palatal shelves fail to meet at midline	J:127720
	thin cortical plate	J:127720