|
XB-GENEPAGE-5766973
slc38a8 solute carrier family 38 member 8
Expression Phenotypes
![]() |
---|
Computed annotations: slc38a8 assayed (5 sources) |
Monarch Ortholog Phenotypes
![]() |
---|
Human (10 sources): Alternating esotropia, Axenfeld anomaly, Foveal hyperpigmentation, Hypoplasia of the fovea, Microphthalmia, Nystagmus, Optic nerve misrouting, Posterior embryotoxon, Reduced visual acuity, Visual impairment |
View all ortholog results at Monarch |