40 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Barx2tm1b(EUCOMM)Hmgu/Barx2tm1b(EUCOMM)Hmgu C57BL/6N-Barx2tm1b(EUCOMM)Hmgu/H	abnormal coat/hair pigmentation	J:211773
	abnormal cornea morphology	J:211773
	abnormal eye morphology	J:211773
	abnormal eyelid morphology	J:211773
	abnormal gait	J:211773
	abnormal tail morphology	J:211773
	abnormal vertebrae morphology	J:211773
	absent vibrissae	J:211773
	corneal opacity	J:211773
	corneal vascularization	J:211773
	eyelids fail to open	J:211773
	increased circulating amylase level	J:211773
	increased circulating aspartate transaminase level	J:211773
	increased circulating bilirubin level	J:211773
	increased circulating creatine kinase level	J:211773
	narrow eye opening	J:211773
	preweaning lethality, incomplete penetrance	J:211773
Barx2tm1Rsd/Barx2tm1Rsd involves: 129/Sv * C57BL/6	abnormal gait	J:187799
	abnormal hair cycle	J:96883
	abnormal motor capabilities/coordination/movement	J:187799
	abnormal muscle fiber morphology	J:187799
	abnormal skeletal muscle fiber morphology	J:187799
	abnormal skeletal muscle morphology	J:187799
	abnormal skin pigmentation	J:96883
	abnormal spine curvature	J:187799
	alopecia	J:187799
	decreased body weight	J:187799
	decreased skeletal muscle fiber diameter	J:187799
	decreased skeletal muscle mass	J:187799
	decreased skeletal muscle weight	J:187799
	disheveled coat	J:96883, J:187799
	enlarged sebaceous gland	J:96883
	eyelids open at birth	J:96883
	impaired skeletal muscle regeneration	J:187799
	increased variability of skeletal muscle fiber size	J:187799
	short hair	J:96883
	short vibrissae	J:96883
	skeletal muscle fiber atrophy	J:187799
	skeletal muscle fibrosis	J:187799
	slow postnatal weight gain	J:187799
	thin diaphragm muscle	J:187799