Bma-spe-42

Brugia malayi

Predicted to be located in membrane. Is an ortholog of C. elegans spe-42. In C. elegans, spe-42 is involved in single fertilization.

Bma-spe-9

Brugia malayi

Predicted to enable calcium ion binding activity. Is an ortholog of C. elegans spe-9. In C. elegans, spe-9 is involved in single fertilization.

Bm8818

Brugia malayi

Is predicted to encode a protein with the following domains: Coiled-coil domain containing 32 and Coiled-coil domain containing protein 32.

Bm6627

Brugia malayi

Is an ortholog of C. elegans Y47G6A.32.

Bm2482

Brugia malayi

Is an ortholog of O. volvulus Ovo-mrpl-32.

Bma-spe-10

Brugia malayi

Predicted to enable palmitoyltransferase activity. Is an ortholog of C. elegans spe-10. In C. elegans, spe-10 is involved in several processes, including amoeboid sperm motility; positive regulation of cell size; and pseudopodium organization.

Bma-spe-6.1

Brugia malayi

Predicted to enable ATP binding activity and protein kinase activity. Is an ortholog of C. elegans spe-6. In C. elegans, spe-6 is involved in male meiosis chromosome separation; regulation of protein localization; and spermatid differentiation.

Bma-spe-6.2

Brugia malayi

Predicted to enable ATP binding activity and protein kinase activity. Is an ortholog of C. elegans spe-6. In C. elegans, spe-6 is involved in male meiosis chromosome separation; regulation of protein localization; and spermatid differentiation.

Bma-spe-15.2

Brugia malayi

Predicted to enable ATP binding activity and cytoskeletal motor activity. Predicted to be part of myosin complex. Is an ortholog of C. elegans spe-15. In C. elegans, spe-15 is involved in organelle localization and spermatid development.

Bma-ceh-32

Brugia malayi

Predicted to enable DNA binding activity. Is an ortholog of C. elegans ceh-32. In C. elegans, ceh-32 is involved in neuron differentiation and post-embryonic animal morphogenesis.