29 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Tnni2tm1.1(KOMP)Vlcg/Tnni2+ C57BL/6N-Tnni2tm1.1(KOMP)Vlcg/Ucd	abnormal skin morphology	J:211773
	decreased circulating glucose level	J:211773
	decreased fasting circulating glucose level	J:211773
	decreased total body fat amount	J:211773
Tnni2tm1.1(KOMP)Vlcg/Tnni2tm1.1(KOMP)Vlcg C57BL/6N-Tnni2tm1.1(KOMP)Vlcg/Ucd	preweaning lethality, complete penetrance	J:211773
Tnni2tm1Sgao/Tnni2+ involves: 129 * ICR	abnormal forelimb morphology	J:228857
	abnormal long bone epiphyseal plate morphology	J:228857
	abnormal long bone hypertrophic chondrocyte zone	J:228857
	decreased angiogenesis	J:228857
	decreased birth weight	J:228857
	decreased body size	J:228857
	decreased bone mineralization	J:228857
	decreased collagen level	J:228857
	decreased osteoblast cell number	J:228857
	decreased osteoblast proliferation	J:228857
	decreased trabecular bone mass	J:228857
	short forelimb	J:228857
	short hindlimb	J:228857
	short vertebral column	J:228857
	slow postnatal weight gain	J:228857
Tnni2tm1Sgao/Tnni2tm1Sgao involves: 129 * ICR	abnormal epiphyseal plate morphology	J:228857
	abnormal forelimb morphology	J:228857
	abnormal intramembranous bone ossification	J:228857
	decreased birth weight	J:228857
	decreased body size	J:228857
	decreased bone mineralization	J:228857
	decreased width of hypertrophic chondrocyte zone	J:228857
	delayed endochondral bone ossification	J:228857
	postnatal lethality, incomplete penetrance	J:228857
	short humerus	J:228857
	short radius	J:228857
	short ulna	J:228857
	small scapula	J:228857