Symbol Name ID |
Aspa
aspartoacylase MGI:87914 |
Darker colors indicate more annotations |
Human Phenotypes | Optic atrophy |
Nystagmus |
Visual impairment |
Blindness |
Disease(s) Associated with ASPA | ||||
Canavan disease |
Mouse Phenotypes | abnormal cornea morphology |
corneal opacity |
abnormal lens morphology |
abnormal retina ganglion layer morphology |
abnormal retina nerve fiber layer morphology |
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Availability | Mouse Genotype | |||||
Aspatm1b(EUCOMM)Wtsi/Aspatm1b(EUCOMM)Wtsi | ||||||
Aspatm1Mata/Aspatm1Mata |
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 04/23/2024 MGI 6.23 |
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