53 phenotypes from 9 alleles in 11 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Atp8a2agil-2J/Atp8a2agil-2J AKR/J-Atp8a2agil-2J/J	abnormal gait	J:140624
	abnormal spinal cord white matter morphology	J:140624
	axonal dystrophy	J:140624
	brain vacuoles	J:140624
	normal hearing/vestibular/ear phenotype	J:140624
	limb grasping	J:140624
	normal vision/eye phenotype	J:140624
Atp8a2agil-3J/Atp8a2agil-3J CBA/J-Atp8a2agil-3J/GrsrJ	abnormal enterocyte morphology	J:176491
	abnormal spinal cord white matter morphology	J:176491
	ataxia	J:176491
	axonal dystrophy	J:176491
	pancreas necrosis	J:176491
	postnatal growth retardation	J:176491
	postnatal lethality	J:176491
Atp8a2agil/Atp8a2agil C3H/HeJ-Atp8a2agil/GrsrJ	abnormal myelination	J:84746
	abnormal spinal cord white matter morphology	J:84746
	ataxia	J:84746
	axonal dystrophy	J:84746
	postnatal growth retardation	J:84746
	postnatal lethality, complete penetrance	J:84746
Atp8a2em1(IMPC)J/Atp8a2+ C57BL/6NJ-Atp8a2em1(IMPC)J/Mmjax	increased circulating glucose level	J:211773
Atp8a2tm1Rsmy/Atp8a2tm1Rsmy involves: 129S6/SvEvTac * C57BL/6NTac	abnormal cone electrophysiology	J:211318
	abnormal retina pigment epithelium morphology	J:211318
	abnormal rod electrophysiology	J:211318
	abnormal voluntary movement	J:211318
	decreased body size	J:211318
	decreased retina photoreceptor cell number	J:211318
	disorganized photoreceptor outer segment	J:211318
	limb grasping	J:211318
	premature death	J:211318
	retina photoreceptor degeneration	J:211318
	short photoreceptor outer segment	J:211318
	thin retina outer nuclear layer	J:211318
	normal vision/eye phenotype	J:211318
Atp8a2wl-2J/Atp8a2wl-2J involves: DBA/2JCri	abnormal motor coordination/balance	J:94340
	abnormal reflex	J:94340
	preweaning lethality, complete penetrance	J:94340
Atp8a2wl-3J/Atp8a2wl-3J CBA/J-Atp8a2wl-3J/J	ataxia	J:29158
	demyelination	J:29158
	lethality at weaning, incomplete penetrance	J:29158
Atp8a2wl-vmd/Atp8a2wl-vmd C3H/HeSnJ-Atp8a2wl-vmd/J	abnormal eating behavior	J:11718
	abnormal startle reflex	J:11718
	axonal dystrophy	J:11718
	cachexia	J:11718
	chromatolysis	J:11718
	decreased body size	J:11718
	disheveled coat	J:11718
	hunched posture	J:11718
	limb grasping	J:11718
	motor neuron degeneration	J:11718
	premature death	J:11718
	short photoreceptor outer segment	J:253580
	short retina cone cell outer segment	J:253580
	tremors	J:11718
Atp8a2wl/Atp8a2+ Not Specified	abnormal motor coordination/balance	J:13068
	ataxia	J:270, J:13068
	demyelination	J:13068, J:15162
Atp8a2wl/Atp8a2wl involves: C57BL/6	cochlear ganglion degeneration	J:211318
	decreased retina photoreceptor cell number	J:211318
	decreased startle reflex	J:211318
	normal hearing/vestibular/ear phenotype	J:211318
	increased or absent threshold for auditory brainstem response	J:211318
	short photoreceptor outer segment	J:211318
	normal vision/eye phenotype	J:211318
Atp8a2wl/Atp8a2wl involves: C57BL/6J	decreased body weight	J:2856
	optic nerve degeneration	J:2856
Atp8a2wl/Atp8a2wl Not Specified	abnormal circulating amino acid level	J:5108
	abnormal enzyme/coenzyme level	J:5108
	abnormal gait	J:13068
	abnormal motor coordination/balance	J:15162
	abnormal reflex	J:13068
	ataxia	J:13068, J:15162
	normal behavior/neurological phenotype	J:13068
	demyelination	J:13068, J:15162
	normal hearing/vestibular/ear phenotype	J:15162
	hypoglycemia	J:14851
	impaired limb coordination	J:15162
	increased circulating tyrosine level	J:5108
	lethality at weaning, complete penetrance	J:13068
	limb grasping	J:13068
	normal nervous system phenotype	J:13068, J:15162
	tremors	J:13068