Automated description from the Alliance of Genome Resources (Release 8.3.0)
Enables D-glucose:proton symporter activity and sucrose:proton symporter activity. Involved in lysosomal lumen pH elevation and melanin biosynthetic process from tyrosine. Acts upstream of or within developmental pigmentation and sucrose transport. Predicted to be active in melanosome membrane. Is expressed in brain; embryo ectoderm; eye; mesenchyme derived from neural crest; and skin. Used to study oculocutaneous albinism. Human ortholog(s) of this gene implicated in oculocutaneous albinism type IV and pigmentation disease. Orthologous to human SLC45A2 (solute carrier family 45 member 2).
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