About Help FAQ

Symbol
Name
ID

Atxn7
ataxin 7
MGI:2179277

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Optic atrophy	Macular degeneration	Pigmentary retinopathy	Nystagmus	Slow saccadic eye movements	Supranuclear ophthalmoplegia	Progressive visual loss
Disease(s) Associated with ATXN7
spinocerebellar ataxia type 7

Mouse Phenotypes		decreased retina photoreceptor cell number	short photoreceptor outer segment	abnormal retina rod cell morphology	retina photoreceptor degeneration	blepharoptosis	thin retina inner plexiform layer	retina outer nuclear layer degeneration
Availability	Mouse Genotype	decreased retina photoreceptor cell number	short photoreceptor outer segment	abnormal retina rod cell morphology	retina photoreceptor degeneration	blepharoptosis	thin retina inner plexiform layer	retina outer nuclear layer degeneration
	Atxn7^tm1Hzo/Atxn7^tm1Hzo
	Atxn7^tm1Hzo/Atxn7⁺

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/16/2024 MGI 6.23