Is predicted to encode a protein with the following domains: Suppressor of white apricot; Alternative splicing regulator; and Suppressor of white apricot, N-terminal domain. Is an ortholog of C. elegans F28C1.1.
Predicted to be involved in transcription initiation at RNA polymerase II promoter. Is an ortholog of C. elegans gtf-2E1. In C. elegans, gtf-2E1 is involved in transcription initiation at RNA polymerase II promoter.
Predicted to be involved in transcription initiation at RNA polymerase II promoter. Predicted to be part of transcription factor TFIIE complex. Is an ortholog of C. elegans gtf-2E2. In C. elegans, gtf-2E2 is involved in transcription initiation at RNA polymerase II promoter.
Predicted to be involved in transcription initiation at RNA polymerase II promoter. Predicted to be part of transcription factor TFIIF complex. Is an ortholog of C. elegans gtf-2F2.
Predicted to be involved in transcription initiation at RNA polymerase III promoter. Predicted to be part of transcription factor TFIIIC complex. Is an ortholog of C. elegans tftc-5.
Predicted to be involved in transcription initiation at RNA polymerase II promoter. Predicted to be part of transcription factor TFIIA complex. Is an ortholog of C. elegans pqn-51.
Predicted to be involved in transcription initiation at RNA polymerase II promoter. Predicted to be part of transcription factor TFIIA complex. Is an ortholog of C. elegans B0336.13 and gtf-2A2.
Predicted to enable RNA polymerase I general transcription initiation factor activity. Predicted to be involved in transcription initiation at RNA polymerase I promoter. Is an ortholog of C. elegans tif-1A.
Predicted to be involved in transcription initiation at RNA polymerase II promoter. Predicted to be part of transcription factor TFIID complex. Is an ortholog of C. elegans taf-7.1 and taf-7.2.