Is an ortholog of C. elegans hlh-29; hlh-28; and hlh-27. In C. elegans, hlh-25 is involved in several processes, including dauer exit; determination of adult lifespan; and negative regulation of transcription by RNA polymerase II.
Predicted to enable protein dimerization activity. Is an ortholog of C. elegans hlh-13. In C. elegans, hlh-13 is involved in dauer exit and response to oxidative stress.
Predicted to enable protein dimerization activity. Is an ortholog of C. elegans hlh-10. In C. elegans, hlh-10 is involved in negative regulation of transcription by RNA polymerase II.
Predicted to enable protein dimerization activity. Is an ortholog of C. elegans hlh-10. In C. elegans, hlh-10 is involved in negative regulation of transcription by RNA polymerase II.
Predicted to enable protein dimerization activity. Is an ortholog of C. elegans hlh-10. In C. elegans, hlh-10 is involved in negative regulation of transcription by RNA polymerase II.
Predicted to enable protein dimerization activity. Is an ortholog of C. elegans hlh-10. In C. elegans, hlh-10 is involved in negative regulation of transcription by RNA polymerase II.
Predicted to enable protein dimerization activity. Is an ortholog of C. elegans hlh-4. In C. elegans, hlh-4 is involved in positive regulation of transcription by RNA polymerase II and response to food.
Predicted to enable protein dimerization activity. Is an ortholog of C. elegans hlh-2. In C. elegans, hlh-2 is involved in several processes, including generation of neurons; regulation of metabolic process; and sex differentiation.
Predicted to enable protein dimerization activity. Is an ortholog of C. elegans hlh-2. In C. elegans, hlh-2 is involved in several processes, including generation of neurons; regulation of metabolic process; and sex differentiation.
Predicted to enable protein dimerization activity. Is an ortholog of C. elegans hlh-2. In C. elegans, hlh-2 is involved in several processes, including generation of neurons; regulation of metabolic process; and sex differentiation.