Is predicted to enable proton-transporting ATP synthase activity, rotational mechanism. Human ortholog(s) of this gene are implicated in mitochondrial complex V (ATP synthase) deficiency nuclear type 3. Is an ortholog of human ATP5F1E (ATP synthase F1 subunit epsilon) and ATP5F1EP2 (ATP synthase F1 subunit epsilon pseudogene 2).
Enables protein domain specific binding activity. Is involved in several processes, including inductive cell migration; multicellular organism development; and pharyngeal pumping. Located in mitochondrion and non-motile cilium. Is expressed in HOB; head; ray neuron type B; and tail. Is an ortholog of human ATP5F1B (ATP synthase F1 subunit beta).
Is predicted to enable ATP binding activity; ATPase-coupled transmembrane transporter activity; and peptide transmembrane transporter activity. Is involved in RNA interference. Is expressed in intestine and muscle cell. Is an ortholog of human ABCB9 (ATP binding cassette subfamily B member 9).