31 phenotypes from 2 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Atxn7em1(IMPC)Bay/Atxn7em1(IMPC)Bay C57BL/6N-Atxn7em1(IMPC)Bay/BayMmucd	abnormal bone structure	J:211773
	decreased prepulse inhibition	J:211773
	decreased total body fat amount	J:211773
	increased bone mineral content	J:211773
	increased startle reflex	J:211773
Atxn7tm1Hzo/Atxn7+ involves: 129S7/SvEvBrd	abnormal Bergmann glial cell morphology	J:113150
	abnormal motor coordination/balance	J:179021
	ataxia	J:179021
	blepharoptosis	J:179021
	kyphosis	J:179021
	premature death	J:179021
	tremors	J:179021
	weight loss	J:179021
Atxn7tm1Hzo/Atxn7+ involves: 129S7/SvEvBrd * C57BL/6	abnormal cerebellum morphology	J:82072
	ataxia	J:82072
	blepharoptosis	J:82072
	decreased brain size	J:82072
	decreased locomotor activity	J:82072
	decreased post-tetanic potentiation	J:82072
	decreased Purkinje cell size	J:82072
	decreased retina photoreceptor cell number	J:82072
	female infertility	J:82072
	impaired coordination	J:82072
	kyphosis	J:82072
	male infertility	J:82072
	myoclonus	J:82072
	premature death	J:82072
	short photoreceptor outer segment	J:82072
	thin retina inner plexiform layer	J:82072
Atxn7tm1Hzo/Atxn7+ involves: 129S7/SvEvBrd * C57BL/6J	abnormal retina rod cell morphology	J:107098
	premature death	J:107098
Atxn7tm1Hzo/Atxn7tm1Hzo involves: 129S7/SvEvBrd	abnormal cerebellum vermis morphology	J:179021
	abnormal gait	J:179021
	ataxia	J:179021
	normal behavior/neurological phenotype	J:179021
	decreased Purkinje cell size	J:179021
	premature death	J:179021
	retina outer nuclear layer degeneration	J:179021
	retina photoreceptor degeneration	J:179021
Atxn7tm1Hzo/Atxn7tm1Hzo involves: 129S7/SvEvBrd * C57BL/6	premature death	J:82072