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Symbol
Name
ID

Ostm1
osteopetrosis associated transmembrane protein 1
MGI:2655574

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Optic atrophy	Optic disc pallor	Proptosis	Mydriasis	Undetectable visual evoked potentials	Nystagmus	Visual impairment	Severely reduced visual acuity
Disease(s) Associated with OSTM1
autosomal recessive osteopetrosis 5

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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