64 phenotypes from 2 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Thbs1tm1.1(KOMP)Vlcg/Thbs1tm1.1(KOMP)Vlcg C57BL/6N-Thbs1tm1.1(KOMP)Vlcg/Ucd	abnormal heart morphology	J:211773
	abnormal liver morphology	J:211773
	abnormal lung morphology	J:211773
	enlarged heart	J:211773
	increased bone mineral content	J:211773
	increased circulating alanine transaminase level	J:211773
Thbs1tm1Hyn/Thbs1tm1Hyn either: (involves: 129S2/SvPas * 129/Sv) or (involves: 129S2/SvPas * C57BL/6)	abnormal cystic duct morphology	J:48446
	abnormal dermal layer morphology	J:48446
	abnormal heart ventricle morphology	J:48446
	abnormal interventricular septum morphology	J:48446
	abnormal kidney corticomedullary boundary morphology	J:48446
	abnormal lung morphology	J:48446
	abnormal lung vasculature morphology	J:48446
	abnormal pancreas morphology	J:48446
	bronchial epithelial hyperplasia	J:48446
	decreased litter size	J:46182
	dilated gallbladder	J:48446
	esophagogastric junction metaplasia	J:48446
	exocrine pancreas hypoplasia	J:48446
	increased club cell number	J:48446
	increased eosinophil cell number	J:46182
	increased leukocyte cell number	J:46182
	increased lymphocyte cell number	J:46182
	increased monocyte cell number	J:46182
	increased neutrophil cell number	J:46182
	kyphosis	J:48446
	lordosis	J:46182
	lung inflammation	J:46182, J:48446
	pancreas inflammation	J:48446
	pancreatic islet hyperplasia	J:48446
	prenatal lethality, incomplete penetrance	J:46182
	pulmonary alveolar hemorrhage	J:48446
	reduced fertility	J:46182
	stomach epithelial hyperplasia	J:48446
	vascular smooth muscle hyperplasia	J:48446
Thbs1tm1Hyn/Thbs1tm1Hyn involves: 129S2/SvPas	abnormal hindlimb morphology	J:133700
	abnormal mitochondrial physiology	J:133700
	abnormal physiological neovascularization	J:133700
	abnormal skin physiology	J:133700
	decreased renal tubule apoptosis	J:104708
	decreased susceptibility to kidney reperfusion injury	J:104708
	normal integument phenotype	J:133700
Thbs1tm1Hyn/Thbs1tm1Hyn involves: 129S2/SvPas * C57BL/6	abnormal conjunctiva goblet cell number	J:153126
	abnormal cornea morphology	J:153126
	abnormal corneal epithelium morphology	J:153126
	abnormal lacrimal gland physiology	J:153126
	abnormal muscle fiber morphology	J:139652
	abnormal systemic arterial blood pressure	J:148948
	normal cellular phenotype	J:139652
	decreased conjunctiva goblet cell number	J:153126
	decreased heart rate	J:148948
	decreased interferon-gamma secretion	J:153126
	decreased pulse pressure	J:148948
	decreased regulatory T cell number	J:153126
	decreased sensitivity to skin irradiation	J:139652
	increased anti-single stranded DNA antibody level	J:153126
	increased CD4-positive, alpha-beta T cell number	J:153126
	increased interleukin-17 secretion	J:153126
	increased lacrimal gland apoptosis	J:153126
	increased mean systemic arterial blood pressure	J:148948
	increased systemic arterial diastolic blood pressure	J:148948
	lacrimal gland inflammation	J:153126
	microphthalmia	J:153126
	normal muscle phenotype	J:139652
	narrow eye opening	J:153126