Slc39a14 - solute carrier family 39 member 14

Predicted to enable anion:cation symporter activity and transition metal ion transmembrane transporter activity. Predicted to be involved in several processes, including negative regulation of cyclic-nucleotide phosphodiesterase activity; transition metal ion homeostasis; and transition metal ion transport. Predicted to act upstream of or within iron ion transport and zinc ion transport. Predicted to be located in apical plasma membrane; basolateral plasma membrane; and bounding membrane of organelle. Predicted to be integral component of membrane. Predicted to be integral component of plasma membrane. Human ortholog(s) of this gene implicated in hypermanganesemia with dystonia 2. Orthologous to human SLC39A14 (solute carrier family 39 member 14). [provided by Alliance of Genome Resources, Apr 2022]