TRANSFAC FACTOR TABLE, Release 2017.2 - public - 2017-06-30, (C) QIAGEN

AC T05122 XX ID T05122 XX DT 21.05.2002 (created); mas. DT 23.06.2015 (updated); sup. CO Copyright (C), QIAGEN. XX FA ChREBP XX SY MIO; mlx interactor; Mlx interactor zeta; wbscr14; Williams-Beuren Syndrome Chromosome Region 14 Protein. XX OS mouse, Mus musculus OC eukaryota; animalia; metazoa; chordata; vertebrata; tetrapoda; mammalia; eutheria; rodentia; myomorpha; muridae; murinae XX GE G004129 Mlxipl. XX CL C0012; bHLH-ZIP; XX SF probably belongs to group B HLH-protein which bind to CACGTG motif (in E-Box) in DNA due to certain residues in DNA-binding domain (arginin at pos. 674) and thus homology to MAX T05056, T00489>, T01567 in this region [1]; XX FF probably transcriptional repressor (e.g. together with MLX) [2]; XX IN T08952 TCFL4-beta; mouse, Mus musculus. IN T19093 TCFL4-gamma; mouse, Mus musculus. XX MX M03789 V$CHREBP_Q6. MX M08802 V$CHREB_Q6_01. XX BS R36355. BS R68485. BS R63068. BS R73473. XX DR TRANSPATH: MO000032967. DR UniProtKB: Q99MZ3; XX RN [1]; RE0017805. RX PUBMED: 9860302. RA Meng X., Lu X., Li Z., Green E. D., Massa H., Trask B. J., Morris C. A., Keating M. T. RT Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes RL Hum. Genet. 103:590-599 (1998). RN [2]; RE0017806. RX PUBMED: 11230181. RA Cairo S., Merla G., Urbinati F., Ballabio A., Reymond A. RT WBSCR14, a gene mapping to the Williams--Beuren syndrome deleted region, is a new member of the Mlx transcription factor network RL Hum. Mol. Genet. 10:617-627 (2001). XX //