70 phenotypes from 3 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ihhtm1.1Dcha/Ihh+ either: (involves: 129S/SvEv * FVB/N) or (involves: 129S/SvEv * FVB/N * ICR)	brachyphalangia	J:147878
	delayed endochondral bone ossification	J:147878
Ihhtm1.1Dcha/Ihhtm1.1Dcha either: (involves: 129S/SvEv * FVB/N) or (involves: 129S/SvEv * FVB/N * ICR)	abnormal appendicular skeleton morphology	J:147878
	abnormal cartilage development	J:147878
	abnormal digit development	J:147878
	abnormal phalanx morphology	J:147878
	brachyphalangia	J:147878
	delayed endochondral bone ossification	J:147878
Ihhtm1Amc/Ihh+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6	decreased long bone epiphyseal plate size	J:99641
Ihhtm1Amc/Ihhtm1Amc involves: 129S1/Sv * 129X1/SvJ	abnormal axial skeleton morphology	J:57297
	abnormal bone mineralization	J:57297
	abnormal bone ossification	J:57297
	abnormal cartilage development	J:57297
	abnormal chondrocyte differentiation	J:57297, J:73071
	abnormal digit morphology	J:57297, J:73071
	abnormal humerus morphology	J:57297
	abnormal joint morphology	J:57297
	abnormal long bone epiphyseal plate proliferative zone	J:57297
	abnormal long bone morphology	J:57297, J:73071
	abnormal rib morphology	J:57297
	abnormal skeleton development	J:73071
	abnormal skeleton morphology	J:57297
	abnormal trabecular bone morphology	J:57297
	chondrodystrophy	J:89228
	decreased body height	J:57297
	decreased chondrocyte proliferation	J:73071
	decreased length of long bones	J:57297
	decreased osteoblast cell number	J:57297
	decreased width of hypertrophic chondrocyte zone	J:57297
	delayed endochondral bone ossification	J:57297
	disproportionate dwarf	J:89228
	domed cranium	J:57297
	embryonic lethality during organogenesis, incomplete penetrance	J:57297
	fused carpal bones	J:57297
	neonatal lethality, complete penetrance	J:57297
	respiratory failure	J:57297
	short fibula	J:73071
	short forelimb	J:57297
	short humerus	J:73071
	short limbs	J:57297, J:73071
	short mandible	J:57297
	short ribs	J:57297
	short scapula	J:73071
	short snout	J:57297
	short tail	J:57297
	short tibia	J:73071
	short ulna	J:73071
	normal vision/eye phenotype	J:78708, J:83530
Ihhtm1Amc/Ihhtm1Amc involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal palatal shelf bone ossification	J:182649
	abnormal palatine bone morphology	J:182649
	abnormal visceral yolk sac morphology	J:128367
	abnormal vitelline vasculature morphology	J:128367
	decreased alkaline phosphatase activity	J:182649
	median cleft palate	J:182649
Ihhtm1Amc/Ihhtm1Amc involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J	abnormal digestive organ placement	J:62158
	abnormal digestive system morphology	J:62158
	abnormal duodenum morphology	J:62158
	abnormal small intestine morphology	J:62158
	abnormal smooth muscle morphology	J:62158
	absent enteric neurons	J:62158
	aganglionic megacolon	J:62158
	annular pancreas	J:62158
	decreased fetal size	J:62158
	normal digestive/alimentary phenotype	J:62158
	megacolon	J:62158
Ihhtm1Blan/Ihhtm1Blan Tg(Col2a1-cre)10Amc/0 involves: 129S4/SvJae * C57BL/6	abnormal basicranium morphology	J:102870
	abnormal bone ossification	J:102870
	abnormal bone structure	J:102870
	abnormal cartilage morphology	J:102870
	abnormal digit morphology	J:102870
	abnormal sternum morphology	J:102870
	abnormal synchondrosis	J:102870
	abnormal trabecular bone morphology	J:102870
	abnormal vertebrae morphology	J:102870
	absent compact bone	J:102870
	chondrodystrophy	J:102870
	delayed endochondral bone ossification	J:102870
	disorganized long bone epiphyseal plate	J:102870
	postnatal lethality	J:102870
	short limbs	J:102870