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CG10804 - uncharacterized protein

Predicted to enable neurotransmitter:sodium symporter activity. Predicted to be involved in amino acid transport; neurotransmitter transport; and sodium ion transmembrane transport. Predicted to be located in membrane. Predicted to be active in plasma membrane. Is expressed in anterior-posterior subdivision of organism; embryonic head sensory system; ganglia; and larval nervous system. Human ortholog(s) of this gene implicated in Hartnup disease and autosomal recessive intellectual developmental disorder 48. Orthologous to several human genes including SLC6A15 (solute carrier family 6 member 15); SLC6A17 (solute carrier family 6 member 17); and SLC6A18 (solute carrier family 6 member 18). [provided by Alliance of Genome Resources, Nov 2024]

Genes similar to CG10804

NCBI Orthologs

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Species Gene Architecture aa