Predicted to enable acetyl-CoA transmembrane transporter activity. Predicted to be involved in acetyl-CoA transmembrane transport. Predicted to be located in membrane. Human ortholog(s) of this gene implicated in hereditary spastic paraplegia 42. Orthologous to human SLC33A1 (solute carrier family 33 member 1).
SGD Description
Putative protein of unknown function; YBR219C is not an essential gene