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Rift - Riboflavin transporter

Predicted to enable riboflavin transmembrane transporter activity. Involved in riboflavin transport. Located in cytosol. Is expressed in several structures, including adult brain cell body rind; amnioserosa; embryonic/larval crystal cell; embryonic/larval midgut; and embryonic/larval midgut primordium. Used to study Brown-Vialetto-Van Laere syndrome. Human ortholog(s) of this gene implicated in Brown-Vialetto-Van Laere syndrome 1; Brown-Vialetto-Van Laere syndrome 2; Fazio-Londe disease; and riboflavin deficiency. Orthologous to several human genes including SLC52A3 (solute carrier family 52 member 3). [provided by Alliance of Genome Resources, Dec 2024]

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Species Gene Architecture aa