60 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Csgalnact1tm1.1Migar/Csgalnact1tm1.1Migar involves: C57BL/6N * C57BL/6NCrlj * CBA/JNCrlj	abnormal basicranium morphology	J:269621
	abnormal cartilage morphology	J:166870
	abnormal chondrocyte morphology	J:269621
	abnormal corneal stroma collagen fibril morphology	J:269621
	abnormal craniofacial development	J:269621
	abnormal craniofacial morphology	J:269621
	abnormal cutaneous collagen fibril morphology	J:269621
	abnormal eye morphology	J:269621
	abnormal glycosaminoglycan level	J:269621
	abnormal intramembranous bone ossification	J:269621
	abnormal nasal cavity morphology	J:269621
	abnormal neurocranium morphology	J:269621
	abnormal palate development	J:269621
	abnormal palate morphology	J:269621
	abnormal scalp morphology	J:269621
	abnormal skeleton morphology	J:269621
	abnormal skin condition	J:269621
	abnormal sphenooccipital synchondrosis	J:269621
	abnormal tail morphology	J:269621
	anophthalmia	J:269621
	axial skeleton hypoplasia	J:166870
	cleft palate	J:269621
	cleft upper lip	J:269621
	normal craniofacial phenotype	J:166870
	decreased body length	J:166870
	decreased body size	J:269621
	decreased body weight	J:166870
	decreased litter size	J:269621
	decreased long bone epiphyseal plate size	J:166870
	decreased maxillary shelf size	J:269621
	decreased width of hypertrophic chondrocyte zone	J:166870
	delayed bone ossification	J:269621
	delayed endochondral bone ossification	J:269621
	delayed intramembranous bone ossification	J:269621
	facial cleft	J:269621
	focal hair loss	J:269621
	joint laxity	J:269621
	lethality throughout fetal growth and development, incomplete penetrance	J:269621
	malocclusion	J:269621
	nasal cartilage hypoplasia	J:269621
	nasal septum hypoplasia	J:269621
	periodontium inflammation	J:269621
	postnatal growth retardation	J:269621
	round head	J:269621
	scoliosis	J:269621
	short face	J:269621
	short femur	J:166870
	short limbs	J:166870
	normal skeleton phenotype	J:166870
	skin atrophy	J:269621
	small mandible	J:269621
	wide cranial sutures	J:269621
Csgalnact1tm1.1Nari/Csgalnact1tm1.1Nari involves: C57BL/6J	abnormal cartilage morphology	J:170410, J:256718
	abnormal long bone epiphyseal plate proliferative zone	J:170410
	decreased long bone epiphyseal plate size	J:170410
	disorganized long bone epiphyseal plate	J:170410
	normal mortality/aging	J:170410
	postnatal growth retardation	J:170410
	proportional dwarf	J:170410
	normal reproductive system phenotype	J:170410
	short humerus	J:170410
	short tibia	J:170410
	normal skeleton phenotype	J:170410
Csgalnact1tm1Lex/Csgalnact1tm1Lex involves: 129S5/SvEvBrd * C57BL/6J	decreased anxiety-related response	J:171883
	normal skeleton phenotype	J:182757