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CG17036 - uncharacterized protein

Predicted to enable vitamin transmembrane transporter activity. Predicted to be involved in transmembrane transport. Predicted to be located in membrane. Predicted to be active in plasma membrane. Is expressed in organism. Human ortholog(s) of this gene implicated in several diseases, including abdominal aortic aneurysm; biotin-responsive basal ganglia disease; cleft lip; dextro-looped transposition of the great arteries; and megaloblastic anemia. Orthologous to several human genes including SLC19A1 (solute carrier family 19 member 1) and SLC19A2 (solute carrier family 19 member 2). [provided by Alliance of Genome Resources, Dec 2024]

Genes similar to CG17036

NCBI Orthologs

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Species Gene Architecture aa