Name

GTF2IRD1 Gene

GTF2I repeat domain containing 1

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]

GTF2IRD1P1 Gene

GTF2I repeat domain containing 1 pseudogene 1

gtf2ird1 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term gtf2ird1 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

GTF2IRD1 Gene Set

From NURSA Protein-Protein Interactions

interacting proteins for GTF2IRD1 from the NURSA Protein-Protein Interactions dataset.

GTF2IRD1 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for GTF2IRD1 from the Pathway Commons Protein-Protein Interactions dataset.

BL5445 (GTF2IRD1) Gene Set

From NURSA Protein Complexes

proteins in the BL5445 (GTF2IRD1) protein complex recovered by IP-MS from the NURSA Protein Complexes dataset.