41 phenotypes from 1 allele in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Mgat2tm1.1Jxm/Mgat2tm1.1Jxm involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal digestion	J:80661
	abnormal facial morphology	J:80661
	abnormal locomotor behavior	J:80661
	abnormal muscle development	J:80661
	abnormal PNS synaptic transmission	J:80661
	anemia	J:80661
	decreased body size	J:80661
	decreased bone mineral density	J:80661
	decreased circulating calcium level	J:80661
	decreased circulating total protein level	J:80661
	decreased fetal size	J:80661
	delayed bone ossification	J:80661
	gastrointestinal hemorrhage	J:80661
	hypoglycemia	J:80661
	increased mean corpuscular volume	J:80661
	increased partial thromboplastin time	J:80661
	kyphoscoliosis	J:80661
	lethality throughout fetal growth and development, incomplete penetrance	J:80661
	normal nervous system phenotype	J:80661
	paralysis	J:80661
	postnatal lethality, complete penetrance	J:80661
	rectal prolapse	J:80661
	reticulocytosis	J:80661
	tremors	J:80661
Mgat2tm1.1Jxm/Mgat2tm1.1Jxm involves: 129S1/Sv * 129X1/SvJ * ICR	abnormal B cell differentiation	J:80661
	abnormal maternal nurturing	J:80661
	abnormal motor coordination/balance	J:80661
	abnormal testis morphology	J:80661
	arrest of male meiosis	J:80661
	azoospermia	J:80661
	decreased body size	J:80661
	decreased grip strength	J:80661
	decreased T cell number	J:80661
	enlarged lymph nodes	J:80661
	enlarged spleen	J:80661
	glomerulonephritis	J:80661
	hematuria	J:80661
	increased urine protein level	J:80661
	male infertility	J:80661
	postnatal lethality, incomplete penetrance	J:80661
	prenatal lethality, incomplete penetrance	J:80661
	reduced female fertility	J:80661