35 phenotypes from 3 alleles in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Asltm1.1Brle/Asltm1.1Brle involves: 129S7/SvEvBrd	no abnormal phenotype detected	J:180208
Asltm1Brle/Asltm1Brle involves: 129S7/SvEvBrd	abnormal coat/ hair morphology	J:180208
	abnormal dermal layer morphology	J:180208
	abnormal erythrocyte morphology	J:180208
	abnormal hair follicle morphology	J:180208
	abnormal myocardial fiber morphology	J:180208
	abnormal nitric oxide homeostasis	J:180208
	abnormal renal glomerulus morphology	J:180208
	acanthocytosis	J:180208
	decreased body weight	J:180208
	decreased circulating alanine transaminase level	J:180208
	decreased circulating arginine level	J:180208
	decreased circulating aspartate transaminase level	J:180208
	decreased creatinine clearance	J:180208
	decreased lymphocyte cell number	J:180208
	decreased spleen germinal center number	J:180208
	decreased vasodilation	J:180208
	epidermal atrophy	J:180208
	increased circulating ammonia level	J:180208
	increased circulating citrulline level	J:180208
	increased macrophage cell number	J:180208
	increased spleen red pulp amount	J:180208
	increased systemic arterial diastolic blood pressure	J:180208
	increased systemic arterial systolic blood pressure	J:180208
	postnatal growth retardation	J:180208
	premature death	J:180208
	small hair follicles	J:180208
	thymus cortex hypoplasia	J:180208
Asltm1Wjc/Asltm1Wjc involves: 129S7/SvEvBrd	abnormal circulating amino acid level	J:101658
	abnormal enzyme/coenzyme activity	J:101658
	abnormal food intake	J:101658
	decreased circulating arginine level	J:101658
	normal homeostasis/metabolism phenotype	J:101658
	increased circulating ammonia level	J:101658
	increased circulating citrulline level	J:101658
	increased circulating glutamine level	J:101658
	lethargy	J:101658
	postnatal lethality, complete penetrance	J:101658