Cbn-vha-12

Caenorhabditis brenneri

Predicted to enable ATP binding activity and proton-transporting ATPase activity, rotational mechanism. Predicted to be involved in ATP metabolic process and proton transmembrane transport. Predicted to be part of proton-transporting V-type ATPase, V1 domain. Is an ortholog of C. elegans vha-12. In C. elegans, vha-12 is involved in several processes, including positive regulation of neurotransmitter secretion; regulation of intracellular pH; and regulation of syncytium formation by plasma membrane fusion.

CBN24709

Caenorhabditis brenneri

Predicted to enable ATP binding activity and proton-transporting ATPase activity, rotational mechanism. Predicted to be involved in ATP metabolic process and proton transmembrane transport. Predicted to be part of proton-transporting V-type ATPase, V1 domain. Is an ortholog of C. elegans vha-12. In C. elegans, vha-12 is involved in several processes, including positive regulation of neurotransmitter secretion; regulation of intracellular pH; and regulation of syncytium formation by plasma membrane fusion.

CBN30182

Caenorhabditis brenneri

Predicted to enable ATP binding activity and proton-transporting ATPase activity, rotational mechanism. Predicted to be involved in ATP metabolic process and proton transmembrane transport. Predicted to be part of proton-transporting V-type ATPase, V1 domain. Is an ortholog of C. elegans vha-12. In C. elegans, vha-12 is involved in several processes, including positive regulation of neurotransmitter secretion; regulation of intracellular pH; and regulation of syncytium formation by plasma membrane fusion.

CBN18302

Caenorhabditis brenneri

Predicted to enable proton-transporting ATPase activity, rotational mechanism. Predicted to be involved in proton transmembrane transport. Predicted to be part of proton-transporting V-type ATPase, V0 domain. Is an ortholog of C. elegans vha-2 and vha-3.

Cbn-vha-6

Caenorhabditis brenneri

Predicted to enable proton-transporting ATPase activity, rotational mechanism. Predicted to be involved in proton transmembrane transport. Predicted to be part of proton-transporting V-type ATPase, V0 domain. Is an ortholog of C. elegans vha-6. In C. elegans, vha-6 is involved in nematode larval development.

Cbn-vha-9

Caenorhabditis brenneri

Predicted to enable proton-transporting ATPase activity, rotational mechanism. Predicted to be involved in proton transmembrane transport. Predicted to be part of proton-transporting V-type ATPase, V1 domain. Is an ortholog of C. elegans vha-9. In C. elegans, vha-9 is involved in lysosomal lumen acidification.

Cbn-vha-11

Caenorhabditis brenneri

Predicted to enable proton-transporting ATPase activity, rotational mechanism. Predicted to be involved in proton transmembrane transport. Predicted to be part of proton-transporting V-type ATPase, V1 domain. Is an ortholog of C. elegans vha-11. In C. elegans, vha-11 is involved in embryo development and ovulation.

Cbn-vha-10

Caenorhabditis brenneri

Predicted to enable proton-transporting ATPase activity, rotational mechanism. Predicted to be involved in proton transmembrane transport. Predicted to be part of vacuolar proton-transporting V-type ATPase complex. Is an ortholog of C. elegans vha-10. In C. elegans, vha-10 is involved in positive regulation of programmed cell death and programmed cell death.

Cbn-vha-17

Caenorhabditis brenneri

Predicted to enable proton-transporting ATPase activity, rotational mechanism. Predicted to be involved in proton transmembrane transport. Predicted to be part of proton-transporting V-type ATPase, V0 domain. Is an ortholog of C. elegans vha-17. In C. elegans, vha-17 is involved in embryo development; embryonic body morphogenesis; and regulation of syncytium formation by plasma membrane fusion.

Cbn-vha-19

Caenorhabditis brenneri

Is predicted to encode a protein with the following domains: V-type proton ATPase subunit S1, luminal domain and V0 complex accessory subunit Ac45. Is an ortholog of C. elegans vha-19. In C. elegans, vha-19 is involved in intracellular water homeostasis; positive regulation of oocyte development; and positive regulation of protein targeting to membrane.