Sequence Detail

ID/Version

Q9JI57 Q80WJ9 Q9EQE7 Q8R4X7 Q80WK0 Q8R4X5 Q80WK1 Q9ESZ7 Q8VHD5 Q8R4X8 Q9ESZ6 Q547E0 Q80WJ8 Q8VI58 Q8R4X6 (UniProt | EBI)

Last sequence update: 2002-05-27
Last annotation update: 2025-02-05

Sequence description from provider

RecName: Full=General transcription factor II-I repeat domain-containing protein 1; Short=GTF2I repeat domain-containing protein 1;AltName: Full=Binding factor for early enhancer;

Provider

SWISS-PROT

Sequence

Polypeptide 1104 aa

Source

Organism mouse

See UniProt | EBI for source

Annotated genes and markers

Follow the symbol links to get more information on the GO terms, expression assays, orthologs, phenotypic alleles, and other information for the genes or markers below.

Type	Symbol	Name	GO Terms	Expression Assays	Orthologs	Phenotypic Alleles
Gene	Gtf2ird1	general transcription factor II I repeat domain-containing 1	11	125	3	323

Sequence references in MGI

J:62856 Bayarsaihan D, et al., Isolation and characterization of BEN, a member of the TFII-I family of DNA-binding proteins containing distinct helix-loop-helix domains. Proc Natl Acad Sci U S A. 2000 Jun 20;97(13):7342-7
J:68983 Durkin ME, et al., Integration of a c-myc Transgene Results in Disruption of the Mouse Gtf2ird1 Gene, the Homologue of the Human GTF2IRD1 Gene Hemizygously Deleted in Williams-Beuren Syndrome. Genomics. 2001 Apr 1;73(1):20-7
J:73801 Bayarsaihan D, et al., Genomic organization of the genes gtf2ird1, gtf2i, and ncf1 at the mouse chromosome 5 region syntenic to the human chromosome 7q11.23 williams syndrome critical region. Genomics. 2002 Jan;79(1):137-43
J:114029 Tussie-Luna MI, et al., Repression of TFII-I-dependent transcription by nuclear exclusion. Proc Natl Acad Sci U S A. 2001 Jul 3;98(14):7789-94