The antiserum was produced against synthesized peptide derived from human GTF2IRD1. AA range:71-120

WBSCR11 Polyclonal Antibody detects endogenous levels of WBSCR11 protein.

GTF2IRD1

General transcription factor II-I repeat domain-containing protein 1

GTF2IRD1 ;
CREAM1 ;
GTF3 ;
MUSTRD1 ;
RBAP2 ;
WBSCR11 ;
WBSCR12 ;
General transcription factor II-I repeat domain-containing protein 1 ;
GTF2I repeat domain-containing protein 1 ;
General transcription factor III ;
MusTRD1/BEN ;
Muscle TFII-I repeat do

The protein encoded by this gene contains five GTF2I-like repeats and each repeat possesses a potential helix-loop-helix (HLH) motif. It may have the ability to interact with other HLH-proteins and function as a transcription factor or as a positive transcriptional regulator under the control of Retinoblastoma protein. This gene plays a role in craniofacial and cognitive development and mutations have been associated with Williams-Beuren syndrome, a multisystem developmental disorder caused by deletion of multiple genes at 7q11.23. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2010],

developmental stage:Highly expressed in developing and regenerating muscles, at the time of myofiber diversification.,Disease:Haploinsufficiency of GTF2IRD1 may be the cause of certain cardiovascular and musculo-skeletal abnormalities observed in Williams-Beuren syndrome (WBS), a rare developmental disorder. It is a contiguous gene deletion syndrome involving genes from chromosome band 7q11.23.,Domain:The N-terminal half may have an activating activity.,Function:May be a transcription regulator involved in cell-cycle progression and skeletal muscle differentiation. May repress GTF2I transcriptional functions, by preventing its nuclear residency, or by inhibiting its transcriptional activation. May contribute to slow-twitch fiber type specificity during myogenesis and in regenerating muscles. Binds troponin I slow-muscle fiber enhancer (USE B1). Binds specifically and with high affinity to the EFG sequences derived from the early enhancer of HOXC8.,PTM:Phosphorylated upon DNA damage, probably by ATM or ATR.,similarity:Belongs to the TFII-I family.,similarity:Contains 5 GTF2I-like repeats.,subunit:Interacts with the retinoblastoma protein (RB1) via its C-terminus.,tissue specificity:Highly expressed in adult skeletal muscle, heart, fibroblast, bone and fetal tissues. Expressed at lower levels in all other tissues tested.,

Nucleus.

>>Basal transcription factors ;
>>cGMP-PKG signaling pathway