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Symbol
Name
ID
Slc38a8
solute carrier family 38, member 8
MGI:2685433
Phenotype annotations related to vision/eye
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+

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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last database update
08/21/2024
MGI 6.24
The Jackson Laboratory