95 phenotypes from 6 alleles in 9 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ilktm1.1(KOMP)Vlcg/Ilk+ C57BL/6N-Ilktm1.1(KOMP)Vlcg/J	abnormal embryo size	J:211773
	hyperactivity	J:211773
	increased circulating phosphate level	J:211773
	increased vertical activity	J:211773
Ilktm1.1(KOMP)Vlcg/Ilktm1.1(KOMP)Vlcg C57BL/6N-Ilktm1.1(KOMP)Vlcg/J	embryonic lethality prior to organogenesis	J:211773
	preweaning lethality, complete penetrance	J:211773
Ilktm1Ref/Ilktm1Ref Not Specified	abnormal basement membrane morphology	J:82761
	abnormal embryonic epiblast morphology	J:82761
	embryonic lethality between implantation and somite formation, complete penetrance	J:82761
Ilktm1Star/Ilktm1Star involves: 129S1/Sv * 129X1/SvJ	abnormal keratinocyte morphology	J:172934
	decreased keratinocyte migration	J:172934
Ilktm1Star/Ilktm1Star Tg(Ckmm-cre)1Lrsn/0 involves: 129S1/Sv * 129X1/SvJ * FVB/N	abnormal heart echocardiography feature	J:112174
	abnormal heart morphology	J:112174
	cardiac interstitial fibrosis	J:112174
	congestive heart failure	J:112174
	decreased cardiac muscle contractility	J:112174
	dilated cardiomyopathy	J:112174
	dilated heart left ventricle	J:112174
	enlarged heart	J:112174
	premature death	J:112174
Ilktm1Star/Ilktm1Star Tg(Col2a1-cre)1Star/? involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal skeleton development	J:84273
	chondrodystrophy	J:84273
	disproportionate dwarf	J:84273
Ilktm1Star/Ilktm1Star Tg(Krt1-15-cre/PGR*)22Cot/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J	delayed wound healing	J:172933
Ilktm1Star/Ilktm1Star Tg(KRT14-cre)1Amc/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	abnormal epidermal layer morphology	J:172934
	abnormal hair follicle development	J:172934
	abnormal hair follicle physiology	J:172934
	abnormal hair growth	J:172934
	abnormal skin pigmentation	J:172934
	acanthosis	J:172934
	blistering	J:172934
	decreased hair follicle number	J:172934
	decreased keratinocyte proliferation	J:172934
	decreased skin tensile strength	J:172934
	postnatal growth retardation	J:172934
	postnatal lethality, complete penetrance	J:172934
	scaly skin	J:172934
	skin edema	J:172934
	skin inflammation	J:172934
	thin skin	J:172934
Ilktm1Star/Ilktm1Star Tg(NPHS2-cre)295Lbh/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	abnormal glomerular capillary morphology	J:129244
	abnormal glomerular filtration barrier function	J:129244
	abnormal kidney morphology	J:129244
	abnormal podocyte morphology	J:129244, J:129286
	abnormal podocyte slit diaphragm morphology	J:129244, J:129286
	abnormal renal glomerulus basement membrane morphology	J:129244, J:129286
	abnormal renal glomerulus morphology	J:129286
	albuminuria	J:129244, J:129286
	decreased body weight	J:129286
	decreased podocyte number	J:129286
	decreased survivor rate	J:129286
	detached podocyte	J:129244, J:129286
	dilated renal tubule	J:129286
	expanded mesangial matrix	J:129244, J:129286
	fused podocyte foot processes	J:129286
	glomerular crescent	J:129244
	glomerulosclerosis	J:129244, J:129286
	increased blood urea nitrogen level	J:129244
	increased circulating cholesterol level	J:129244
	increased circulating creatinine level	J:129286
	increased kidney apoptosis	J:129286
	increased podocyte apoptosis	J:129286
	increased renal glomerulus basement membrane thickness	J:129244, J:129286
	increased urine protein level	J:129244, J:129286
	kidney failure	J:129244, J:129286
	podocyte foot process effacement	J:129244, J:129286
	podocyte microvillus transformation	J:129244, J:129286
	premature death	J:129244, J:129286
	renal glomerular synechia	J:129244
	renal glomerulus hypertrophy	J:129286
	renal interstitial fibrosis	J:129244, J:129286
	renal tubule atrophy	J:129244
	tubulointerstitial nephritis	J:129244, J:129286
Ilktm1Star/Ilktm2Star Tg(Acp5-cre)1Star/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal osteoclast physiology	J:197593
	normal craniofacial phenotype	J:197593
	normal growth/size/body region phenotype	J:197593
	increased bone volume	J:197593
	increased osteoclast cell number	J:197593
	increased trabecular bone thickness	J:197593
Ilktm3Ref/Ilktm3Ref involves: 129S1/Sv * 129X1/SvJ	abnormal ureteric bud morphology	J:154054
Ilktm3Ref/Ilktm3Ref Tg(Col2a1-cre)1Asz/0 involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	abnormal cell adhesion	J:110783
	abnormal cell cycle	J:110783
	abnormal chest morphology	J:110783
	abnormal long bone hypertrophic chondrocyte zone	J:110783
	cleft palate	J:110783
	decreased cell proliferation	J:110783
	decreased fetal size	J:110783
	decreased long bone epiphyseal plate size	J:110783
	disorganized long bone epiphyseal plate	J:110783
	disproportionate dwarf	J:110783
	neonatal lethality, complete penetrance	J:110783
	pulmonary hypoplasia	J:110783
Ilktm10.1Ref/Ilktm10.1Ref B6.129(Cg)-Ilktm10.1Ref	absent vitelline blood vessels	J:199658
	delayed embryo turning	J:199658
	embryonic growth retardation	J:199658
	embryonic lethality between somite formation and embryo turning, incomplete penetrance	J:199658
	embryonic lethality during organogenesis, complete penetrance	J:199658