36 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Cdo1tm1.1Mhst/Cdo1tm1.1Mhst involves: C57BL/6	abnormal axial skeleton morphology	J:182195
	abnormal cranium morphology	J:182195
	abnormal digit morphology	J:182195
	abnormal eyelid morphology	J:182195
	abnormal fertility/fecundity	J:182195
	abnormal forelimb morphology	J:182195
	abnormal lacrimal gland physiology	J:182195
	abnormal limb posture	J:182195
	abnormal motor capabilities/coordination/movement	J:182195
	abnormal nasal bone morphology	J:182195
	abnormal nose morphology	J:182195
	abnormal outer ear morphology	J:182195
	abnormal pulmonary alveolar system morphology	J:182195
	abnormal pulmonary artery morphology	J:182195
	abnormal pulmonary collagen fibril morphology	J:182195
	decreased birth weight	J:182195
	decreased body length	J:182195
	decreased bone mineral density	J:182195
	decreased circulating glucose level	J:182195
	decreased circulating insulin-like growth factor I level	J:182195
	decreased locomotor activity	J:182195
	decreased taurine level	J:182195
	delayed eyelid opening	J:182195
	increased circulating cysteine level	J:182195
	increased cysteine level	J:182195
	increased food intake	J:182195
	kyphosis	J:182195
	male infertility	J:182195
	malocclusion	J:182195
	narrow eye opening	J:182195
	postnatal lethality, incomplete penetrance	J:182195
	slow postnatal weight gain	J:182195
Cdo1tm1Mhst/Cdo1tm1Mhst Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+ involves: C57BL/6 * DBA	abnormal blood homeostasis	J:186922
	abnormal homeostasis	J:186922
	decreased circulating cysteine level	J:186922
	decreased cysteine level	J:186922