33 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Csf1op/Csf1op Galctwi/Galctwi involves: C3HeB/Fe * C57BL/6J * CE/J	abnormal forebrain morphology	J:170081
	abnormal oligodendrocyte morphology	J:170081
	abnormal oligodendrocyte physiology	J:170081
	absent incisors	J:170081
	decreased body size	J:170081
	decreased oligodendrocyte number	J:170081
	decreased oligodendrocyte progenitor number	J:170081
	demyelination	J:170081
	domed cranium	J:170081
	hindlimb paralysis	J:170081
	impaired macrophage chemotaxis	J:170081
	premature death	J:170081
	tremors	J:170081
	weight loss	J:170081
Galctwi/Galctwi Glb1tm1Adz/Glb1+ involves: 129P2/OlaHsd * C57BL/6J * CE/J	abnormal lipid level	J:63197
	demyelination	J:63197
	normal immune system phenotype	J:63197
	induced hyperactivity	J:63197
	normal liver/biliary system phenotype	J:63197
	neurodegeneration	J:63197
	premature death	J:63197
	seizures	J:63197
Galctwi/Galctwi Glb1tm1Adz/Glb1tm1Adz involves: 129P2/OlaHsd * C57BL/6J * CE/J	abnormal lipid level	J:63197
	abnormal liver morphology	J:63197
	abnormal macrophage physiology	J:63197
	abnormal renal glomerular capsule morphology	J:63197
	abnormal renal tubule epithelium morphology	J:63197
	demyelination	J:63197
	enlarged liver	J:63197
	enlarged spleen	J:63197
	premature death	J:63197
Galctwi/Galctwi Hpgdstm1Urad/Hpgdstm1Urad B6.Cg-Hpgdstm1Urad Galctwi	abnormal astrocyte morphology	J:108359
	ataxia	J:108359
	decreased apoptosis	J:108359
	premature death	J:108359
Galctwi/Galctwi Il6tm1Kopf/Il6tm1Kopf involves: 129S2/SvPas * C57BL/6J * CE/J	abnormal blood-brain barrier function	J:56656
	abnormal cerebellum white matter morphology	J:56656
	abnormal tumor necrosis factor level	J:56656
	gliosis	J:56656
	tremors	J:56656
Galctwi/Galctwi Ptgdrtm1Sna/Ptgdrtm1Sna B6.Cg-Galctwi Ptgdrtm1Sna	abnormal astrocyte morphology	J:108359
	ataxia	J:108359
	premature death	J:108359