56 phenotypes from 8 alleles in 11 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Mgrn1em1(IMPC)Tcp/Mgrn1+ C57BL/6NCrl-Mgrn1em1(IMPC)Tcp/Tcp	abnormal uterus morphology	J:211773
	decreased lymphocyte cell number	J:211773
	enlarged urinary bladder	J:211773
	increased freezing behavior	J:211773
	increased heart weight	J:211773
	increased lymphocyte cell number	J:211773
	increased neutrophil cell number	J:211773
	increased spleen weight	J:211773
	shortened QRS complex duration	J:211773
Mgrn1em1(IMPC)Tcp/Mgrn1em1(IMPC)Tcp C57BL/6NCrl-Mgrn1em1(IMPC)Tcp/Tcp	abnormal auditory brainstem response	J:211773
	abnormal bone structure	J:211773
	abnormal coat/hair pigmentation	J:211773
	abnormal cranium morphology	J:211773
	abnormal ear morphology	J:211773
	abnormal pancreas morphology	J:211773
	abnormal skin coloration	J:211773
	abnormal skin morphology	J:211773
	abnormal sternum morphology	J:211773
	decreased bone mineral content	J:211773
	enlarged lymph nodes	J:211773
	increased circulating alkaline phosphatase level	J:211773
	increased circulating bilirubin level	J:211773
	increased mean corpuscular hemoglobin	J:211773
	preweaning lethality, incomplete penetrance	J:211773
Mgrn1Gt(XC712)Byg/Mgrn1Gt(XC712)Byg involves: 129P2/OlaHsd * 129S1/SvImJ	abnormal coat/hair pigmentation	J:119125
	normal embryo phenotype	J:116645
Mgrn1md-2J/Mgrn1md-2J C3H/HeJ-Mgrn1md-2J	abnormal coat/hair pigmentation	J:119125
Mgrn1md-2J/Mgrn1md-2J involves: 129S1/SvImJ * C3H/HeJ	abnormal coronary sinus morphology	J:116645
	abnormal heart and great artery attachment	J:116645
	abnormal left subclavian artery morphology	J:116645
	abnormal left-right axis patterning	J:116645
	atrial septal defect	J:116645
	congestive heart failure	J:116645
	dextrocardia	J:116645
	double outlet right ventricle	J:116645
	hemorrhage	J:116645
	left pulmonary isomerism	J:116645
	lung situs inversus	J:116645
	mesocardia	J:116645
	pericardial effusion	J:116645
	perinatal lethality, incomplete penetrance	J:116645
	pleural effusion	J:116645
	postnatal lethality, incomplete penetrance	J:116645
	prenatal lethality, incomplete penetrance	J:116645
	right aortic arch	J:116645
	situs inversus	J:116645
	thin myocardium	J:116645
	ventricular septal defect	J:116645
Mgrn1md-4J/Mgrn1md-4J C3H/HeJ-Mgrn1md-4J	abnormal coat/hair pigmentation	J:98126
	darkened coat color	J:98126
Mgrn1md-5J/Mgrn1md-5J C3H/HeJ-Mgrn1md-5J	abnormal coat/hair pigmentation	J:78379
	darkened coat color	J:78379
Mgrn1md-6J/Mgrn1md-6J C3H/HeJ-Mgrn1md-6J	abnormal coat/hair pigmentation	J:78379
	darkened coat color	J:78379
Mgrn1md-nc/Mgrn1md-nc 129S1.Cg-Mgrn1md-nc	prenatal lethality, complete penetrance	J:116645
Mgrn1md-nc/Mgrn1md-nc C3.Cg-Mgrn1md-nc	prenatal lethality	J:116645
Mgrn1md-nc/Mgrn1md-nc involves: 101/H * C3H/HeH	abnormal coronary sinus morphology	J:116645
	abnormal heart and great artery attachment	J:116645
	abnormal left subclavian artery morphology	J:116645
	abnormal left-right axis patterning	J:116645
	astrocytosis	J:81466
	atrial septal defect	J:116645
	brain vacuoles	J:81466
	congestive heart failure	J:116645
	curly vibrissae	J:15051, J:81466, J:116645
	darkened coat color	J:15051, J:81466
	decreased litter size	J:81466
	dextrocardia	J:116645
	double outlet right ventricle	J:116645
	hemorrhage	J:116645
	left pulmonary isomerism	J:116645
	lung situs inversus	J:116645
	mesocardia	J:116645
	muscle weakness	J:81466
	pericardial effusion	J:116645
	perinatal lethality, incomplete penetrance	J:116645
	pleural effusion	J:116645
	postnatal lethality, incomplete penetrance	J:116645
	premature death	J:15072, J:116645
	prenatal lethality, incomplete penetrance	J:116645
	right aortic arch	J:116645
	situs inversus	J:116645
	spongiform encephalopathy	J:81466, J:116645
	thin myocardium	J:116645
	ventricular septal defect	J:116645
Mgrn1md/Mgrn1md C3H/HeJ-Mgrn1md/J	darkened coat color	J:81466