Symbol Name ID |
Ostm1
osteopetrosis associated transmembrane protein 1 MGI:2655574 |
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 |
Mouse Phenotypes | eye inflammation |
delayed eyelid opening |
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Availability | Mouse Genotype | ||
Ostm1gl/Ostm1gl |
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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last database update 04/09/2024 MGI 6.23 |
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