SLC9A3R1 (solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 1) is a protein-coding gene. Diseases associated with SLC9A3R1 include nephrolithiasis/osteoporosis, hypophosphatemic, 2, and cystic fibrosis, and among its related super-pathways are Regulation of CFTR activity (norm and CF) and Clathrin-dependent protein traffic. GO annotations related to this gene include beta-catenin binding and receptor binding. An important paralog of this gene is SLC9A3R2.
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