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Symbol
Name
ID

Snx10
sorting nexin 10
MGI:1919232

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Optic atrophy	Unilateral microphthalmos	Visual loss
Disease(s) Associated with SNX10
autosomal recessive osteopetrosis 8

Mouse Phenotypes		abnormal eye morphology
Availability	Mouse Genotype	abnormal eye morphology
	Snx10^em1(IMPC)Mbp/Snx10^em1(IMPC)Mbp

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)
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