55 phenotypes from 6 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fig4plt1/Fig4plt1 B6.Cg-Fig4plt1	abnormal heart atrium morphology	J:190368
Fig4plt1/Fig4plt1 involves: 129 * C3H * C57BL/6J * CAST/Ei * SJL	abnormal brain morphology	J:173446
	abnormal myelin sheath morphology	J:173446
	abnormal sciatic nerve morphology	J:173446
	astrocytosis	J:173446
	decreased nerve conduction velocity	J:173446
	diluted coat color	J:173446
	hypopigmentation	J:173446
	neurodegeneration	J:173446
	neuron degeneration	J:173446
	premature death	J:173446
	spongiform encephalopathy	J:173446
Fig4plt1/Fig4plt1 involves: 129P2/OlaHsd * C3H * C57BL/6 * CAST/Ei * SJL	abnormal action potential	J:122737
	abnormal gait	J:122737
	abnormal hair follicle morphology	J:122737
	abnormal limb posture	J:122737
	abnormal melanosome morphology	J:122737
	abnormal motor capabilities/coordination/movement	J:185989
	abnormal motor neuron morphology	J:122737
	abnormal nerve conduction	J:122737, J:185989
	abnormal nervous system morphology	J:185989
	abnormal sciatic nerve morphology	J:122737
	astrocytosis	J:185989
	decreased body size	J:122737
	decreased body weight	J:122737
	decreased hair follicle number	J:122737
	demyelination	J:185989
	diluted coat color	J:122737, J:185989
	impaired coordination	J:122737
	muscle weakness	J:122737
	neuron degeneration	J:122737
	premature death	J:122737, J:185989
	spleen hypoplasia	J:122737
	spongiform encephalopathy	J:185989
	tremors	J:122737, J:185989
Fig4plt1/Fig4plt1 involves: 129P2/OlaHsd * C3H * SJL	abnormal bone marrow cell morphology/development	J:203638
	abnormal bone ossification	J:203638
	abnormal bone structure	J:203638
	abnormal compact bone morphology	J:203638
	abnormal craniofacial morphology	J:203638
	abnormal osteoblast morphology	J:203638
	abnormal skeleton morphology	J:203638
	abnormal trabecular bone morphology	J:203638
	decreased body weight	J:203638
	decreased bone trabecula number	J:203638
	decreased bone volume	J:203638
	decreased compact bone thickness	J:203638
	decreased length of long bones	J:203638
	decreased trabecular bone connectivity density	J:203638
	decreased trabecular bone volume	J:203638
	normal limbs/digits/tail phenotype	J:203638
	long incisors	J:203638
	postnatal growth retardation	J:203638
	small clavicle	J:203638
Fig4plt1/Fig4plt1 Tg(ACTB-Fig4*I41T)705Mm/0 involves: 129 * C3H * C57BL/6J * CAST/Ei * SJL	abnormal brain morphology	J:173446
	astrocytosis	J:173446
	decreased nerve conduction velocity	J:173446
	diluted coat color	J:173446
	domed cranium	J:173446
	enlarged lateral ventricles	J:173446
	hydrocephaly	J:173446
	hypopigmentation	J:173446
	normal nervous system phenotype	J:173446
	neurodegeneration	J:173446
	premature death	J:173446
	spongiform encephalopathy	J:173446
Fig4plt1/Fig4plt1 Tg(ACTB-Fig4*I41T)721Mm/0 involves: 129 * C3H * C57BL/6J * CAST/Ei * SJL	abnormal brain morphology	J:173446
	astrocytosis	J:173446
	decreased nerve conduction velocity	J:173446
	enlarged lateral ventricles	J:173446
	hydrocephaly	J:173446
	hypopigmentation	J:173446
	normal mortality/aging	J:173446
	normal nervous system phenotype	J:173446
	neurodegeneration	J:173446
	spongiform encephalopathy	J:173446
Fig4plt1/Fig4plt1 Tg(Eno2-Fig4)#Mm/? involves: 129P2/OlaHsd * C3H * C57BL/6 * CAST/Ei * SJL	abnormal postnatal growth	J:185989
	normal nervous system phenotype	J:185989
	premature death	J:185989
Fig4plt1/Fig4plt1 Tg(GFAP-Fig4)#Mm/? involves: 129P2/OlaHsd * C3H * C57BL/6 * CAST/Ei * SJL	abnormal motor capabilities/coordination/movement	J:185989
	abnormal postnatal growth	J:185989
	demyelination	J:185989
	normal nervous system phenotype	J:185989
	premature death	J:185989
	spongiform encephalopathy	J:185989
	tremors	J:185989
Fig4tm1.1Mm/Fig4tm1.1Mm Tg(Syn1-cre)671Jxm/? involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	abnormal motor capabilities/coordination/movement	J:185989
	astrocytosis	J:185989
	decreased body weight	J:185989
	normal integument phenotype	J:185989
	limb grasping	J:185989
	premature death	J:185989
	spongiform encephalopathy	J:185989