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slc19a3b - solute carrier family 19 member 3b

Predicted to enable vitamin transmembrane transporter activity. Predicted to be involved in transmembrane transport. Predicted to act upstream of or within vitamin transport. Predicted to be located in membrane. Predicted to be integral component of membrane. Predicted to be active in plasma membrane. Human ortholog(s) of this gene implicated in biotin-responsive basal ganglia disease. Orthologous to human SLC19A3 (solute carrier family 19 member 3). [provided by Alliance of Genome Resources, Apr 2022]

Genes similar to slc19a3b

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Species Gene Architecture aa