Symbol Name ID |
Slc38a8
solute carrier family 38, member 8 MGI:2685433 |
Darker colors indicate more annotations |
Human Phenotypes | Posterior embryotoxon |
Astigmatism |
Axenfeld anomaly |
Optic nerve misrouting |
Foveal hyperpigmentation |
Hypoplasia of the fovea |
Microphthalmia |
Strabismus |
Alternating esotropia |
Nystagmus |
Reduced visual acuity |
Disease(s) Associated with SLC38A8 | |||||||||||
foveal hypoplasia 2 |
Mouse Phenotypes | abnormal choroid pigmentation |
abnormal iris pigmentation |
abnormal retina pigment epithelium morphology |
decreased a-wave amplitude |
decreased b-wave amplitude |
decreased visual acuity |
|
Availability | Mouse Genotype | ||||||
Slc38a8em1Lmon/Slc38a8em1Lmon | |||||||
Slc38a8em1Lmon/Slc38a8+ |
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 08/21/2024 MGI 6.24 |
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