33 phenotypes from 3 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Lumtm1.1(KOMP)Vlcg/Lum+ C57BL/6N-Lumtm1.1(KOMP)Vlcg/Ucd	increased circulating alanine transaminase level	J:211773
	increased circulating aspartate transaminase level	J:211773
Lumtm1.1(KOMP)Vlcg/Lumtm1.1(KOMP)Vlcg C57BL/6N-Lumtm1.1(KOMP)Vlcg/Ucd	abnormal tail morphology	J:211773
	preweaning lethality, complete penetrance	J:211773
Lumtm1Chak/Lumtm1Chak involves: 129S/Sv * CD-1	abnormal apoptosis	J:89489
	abnormal cornea morphology	J:48068, J:70246
	abnormal cornea posterior stroma morphology	J:64730
	abnormal corneal stroma development	J:48068, J:81616
	abnormal corneal stroma morphology	J:48068, J:64730
	abnormal dermal layer morphology	J:48068
	abnormal tendon morphology	J:65867
	bruising	J:48068
	normal cardiovascular system phenotype	J:48068
	corneal opacity	J:48068, J:64730
	decreased body size	J:48068
	decreased body weight	J:48068
	decreased corneal stroma thickness	J:64730, J:81616
	decreased fibroblast apoptosis	J:89489
	decreased skin tensile strength	J:48068
	normal digestive/alimentary phenotype	J:48068
	increased corneal light-scattering	J:64730, J:81616
	increased fibroblast proliferation	J:89489
	loose skin	J:48068
	sclera thinning	J:83544
	skin lesions	J:48068
Lumtm1Wwk/Lumtm1Wwk involves: 129P2/OlaHsd	abnormal inflammatory response	J:128992
	corneal opacity	J:128992
	decreased cornea thickness	J:128992
	decreased neutrophil cell number	J:128992
Lumtm1Wwk/Lumtm1Wwk involves: 129P2/OlaHsd * C57BL/6J	abnormal coat appearance	J:60203
	abnormal cornea posterior stroma morphology	J:60203
	abnormal corneal wound healing	J:60203
	abnormal skin condition	J:60203
	corneal opacity	J:60203
	delayed wound healing	J:60203
	reduced male fertility	J:60203