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Gm587


Official Full Name
solute carrier family 38, member 8
Organism
Mus musculus
Gene ID
234788
Background
Predicted to enable L-amino acid transmembrane transporter activity. Acts upstream of or within nervous system development; retinal pigment epithelium development; and visual perception. Predicted to be located in axon and cell cortex. Predicted to be active in membrane. Used to study foveal hypoplasia 2. Human ortholog(s) of this gene implicated in foveal hypoplasia 2. Orthologous to human SLC38A8 (solute carrier family 38 member 8). [provided by Alliance of Genome Resources, Feb 2025]
Synonyms
Slc38a8; Gm587

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