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XB-GENEPAGE-5766973
slc38a8 solute carrier family 38 member 8
Expression Phenotypes
Gene expression phenotype annotations where the gene of interest has been
disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from
differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1,
FDR <= 0.05 and an absolute LogFC >= 2.
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| Computed annotations: slc38a8 assayed (5 sources) |
| Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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| 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 |
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View all ortholog results at Monarch |