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slc34a1a - solute carrier family 34 member 1a

Predicted to enable sodium:phosphate symporter activity. Predicted to be involved in cellular phosphate ion homeostasis and sodium-dependent phosphate transport. Predicted to be located in plasma membrane. Predicted to be integral component of membrane. Predicted to be active in apical plasma membrane; brush border; and vesicle. Human ortholog(s) of this gene implicated in several diseases, including Fanconi syndrome (multiple); chronic kidney disease; hereditary hypophosphatemic rickets with hypercalciuria; hypophosphatemic nephrolithiasis/osteoporosis 1; and nephrolithiasis. Orthologous to human SLC34A1 (solute carrier family 34 member 1). [provided by Alliance of Genome Resources, Apr 2022]

Genes similar to slc34a1a

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Species Gene Architecture aa