37 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Xirp2tm1.1Itl/Xirp2tm1.1Itl involves: FVB/N	no abnormal phenotype detected	J:170869
Xirp2tm1Itl/Xirp2tm1Itl Not Specified	abnormal response/metabolism to endogenous compounds	J:170869
	cardiac hypertrophy	J:170869
	normal cardiovascular system phenotype	J:170869
	increased heart weight	J:170869
	increased myocardial fiber size	J:170869
Xirp2tm1Jl/Xirp2tm1Jl B6.129-Xirp2tm1Jl	abnormal atrioventricular bundle morphology	J:255706
	abnormal cardiovascular system physiology	J:158491
	abnormal heart electrocardiography waveform feature	J:255706
	abnormal heart left ventricle morphology	J:158491
	abnormal heart right ventricle morphology	J:158491
	abnormal heart shape	J:158491
	abnormal impulse conducting system conduction	J:255706
	abnormal intercalated disk morphology	J:158491
	abnormal myocardial fiber currents	J:255706
	abnormal myocardial fiber morphology	J:158491
	abnormal Purkinje fiber morphology	J:255706
	abnormal trabecula carnea morphology	J:158491
	atrioventricular block	J:255706
	decreased acetylcholinesterase activity	J:255706
	decreased birth weight	J:158491
	decreased body weight	J:158491
	decreased diastolic filling velocity	J:158491
	decreased heart weight	J:158491
	decreased liver weight	J:158491
	decreased locomotor activity	J:158491
	decreased myocardial fiber size	J:158491
	disorganized myocardium	J:158491
	increased cardiomyocyte apoptosis	J:158491
	muscular ventricular septal defect	J:158491
	pallor	J:158491
	postnatal growth retardation	J:158491
	postnatal lethality, complete penetrance	J:158491
	prolonged PR interval	J:255706
	prolonged QT interval	J:255706
	slow postnatal weight gain	J:158491
	ventricular myocardium compact layer hypoplasia	J:158491