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Overview
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Background
SLC30A1 (Solute Carrier Family 30 Member 1) is a Protein Coding gene. Diseases associated with SLC30A1 include Acrodermatitis Enteropathica, Zinc-Deficiency Type and Epidermodysplasia Verruciformis 1. Among its related pathways are Metal ion SLC transporters and Mineral absorption. Gene Ontology (GO) annotations related to this gene include cation transmembrane transporter activity and calcium channel inhibitor activity. An important paralog of this gene is SLC30A10.
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