53 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Lama4tm1.1(KOMP)Vlcg/Lama4tm1.1(KOMP)Vlcg C57BL/6N-Lama4tm1.1(KOMP)Vlcg/Ucd	abnormal coat/hair pigmentation	J:211773
	abnormal skin morphology	J:211773
	corneal opacity	J:211773
	increased basophil cell number	J:211773
	increased circulating alkaline phosphatase level	J:211773
	increased heart weight	J:211773
	preweaning lethality, incomplete penetrance	J:211773
Lama4tm1Ktry/Lama4tm1Ktry B6.129X1-Lama4tm1Ktry	abnormal axon radial sorting	J:98348
	abnormal capillary morphology	J:105789
	abnormal dorsal spinal root morphology	J:98348
	abnormal myelin sheath morphology	J:98348
	abnormal myelination	J:98086, J:98348
	abnormal myocardial fiber morphology	J:105789
	abnormal sciatic nerve morphology	J:98348
	abnormal sinus arrhythmia	J:105789
	abnormal ventral spinal root morphology	J:98348
	ataxia	J:98348
	cardiac hypertrophy	J:105789
	cardiac interstitial fibrosis	J:105789
	cardiac ischemia	J:105789
	cardiomyopathy	J:105789
	decreased heart rate	J:105789
	decreased Schwann cell number	J:98086
	decreased ventricle muscle contractility	J:105789
	dilated capillary	J:105789
	dilated heart left ventricle	J:105789
	enlarged heart	J:105789
	heart left ventricle hypertrophy	J:105789
	hemorrhage	J:98348
	hypoxia	J:105789
	impaired swimming	J:98348
	increased myocardial fiber size	J:105789
	increased susceptibility to induced morbidity/mortality	J:105789
	limb grasping	J:98086
	myocardial fiber degeneration	J:105789
	poor circulation	J:105789
	tremors	J:98348
Lama4tm1Ktry/Lama4tm1Ktry either: B6.129X1-Lama4tm1Ktry or (involves: 129X1/SvJ * C57BL/6)	abnormal blood vessel morphology	J:74287
	abnormal capillary morphology	J:74287
	abnormal circulating bilirubin level	J:74287
	anemia	J:74287
	decreased body weight	J:74287
	decreased erythrocyte cell number	J:74287
	decreased hematocrit	J:74287
	decreased hemoglobin content	J:74287
	dilated capillary	J:74287
	hemorrhage	J:74287
	impaired balance	J:74287
	impaired basement membrane formation	J:74287
	impaired limb coordination	J:74287
	internal hemorrhage	J:74287
	jaundice	J:74287
	lethargy	J:74287
	neonatal lethality, incomplete penetrance	J:74287
	pallor	J:74287
	reticulocytosis	J:74287