Version 5.4
| Mus musculus Gene: Gtf2ird1 | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Summary | |||||||||
| InnateDB Gene | IDBG-202722.6 | ||||||||
| Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||
| Gene Symbol | Gtf2ird1 | ||||||||
| Gene Name | general transcription factor II I repeat domain-containing 1 | ||||||||
| Synonyms | 1700012P16Rik; BEN; Cream1; ESTM9; Gtf2il; GTF3; MusTRD1; Tg(Alb1-Myc)166.8Sst; WBSCR11; X83320 | ||||||||
| Species | Mus musculus | ||||||||
| Ensembl Gene | ENSMUSG00000023079 | ||||||||
| Encoded Proteins |
general transcription factor II I repeat domain-containing 1
general transcription factor II I repeat domain-containing 1
general transcription factor II I repeat domain-containing 1
general transcription factor II I repeat domain-containing 1
general transcription factor II I repeat domain-containing 1
general transcription factor II I repeat domain-containing 1
general transcription factor II I repeat domain-containing 1
general transcription factor II I repeat domain-containing 1
general transcription factor II I repeat domain-containing 1
|
||||||||
| Protein Structure | |||||||||
| Useful resources | Stemformatics EHFPI ImmGen | ||||||||
| Entrez Gene | |||||||||
| Summary |
This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000006704:
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] |
||||||||
| Gene Information | |||||||||
| Type | Protein coding | ||||||||
| Genomic Location | Chromosome 5:134357669-134456716 | ||||||||
| Strand | Reverse strand | ||||||||
| Band | G2 | ||||||||
| Transcripts | |||||||||
| Interactions | |||||||||
| Number of Interactions |
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 8 interaction(s) predicted by orthology.
|
||||||||
| Gene Ontology | |||||||||
Molecular Function |
|
||||||||
| Biological Process |
|
||||||||
| Cellular Component |
|
||||||||
| Orthologs | |||||||||
|
Species
Homo sapiens
Bos taurus
|
Gene ID
Gene Order
Not yet available
|
||||||||
| Pathways | |||||||||
| NETPATH | |||||||||
| REACTOME | |||||||||
| KEGG |
Basal transcription factors pathway
|
||||||||
| INOH | |||||||||
| PID NCI | |||||||||
| Pathway Predictions based on Human Orthology Data | |||||||||
| NETPATH | |||||||||
| REACTOME | |||||||||
| KEGG |
Basal transcription factors pathway
|
||||||||
| INOH | |||||||||
| PID NCI | |||||||||
| Cross-References | |||||||||
| SwissProt | |||||||||
| TrEMBL | |||||||||
| UniProt Splice Variant | |||||||||
| Entrez Gene | |||||||||
| UniGene | Mm.332735 Mm.437004 | ||||||||
| RefSeq | NM_001081462 NM_001081463 NM_001081464 NM_001081465 NM_001081466 NM_001081467 NM_001081468 NM_001081469 NM_001081470 NM_001244936 NM_020331 XM_006504457 XM_006504458 XM_006504459 XM_006504460 XM_006504461 XM_006504464 XM_006504465 XM_006504466 XM_006504467 XM_006504470 | ||||||||
| OMIM | |||||||||
| CCDS | CCDS39302 CCDS39303 CCDS39304 CCDS39305 CCDS39306 CCDS39307 CCDS51657 | ||||||||
| HPRD | |||||||||
| IMGT | |||||||||
| MGI ID | |||||||||
| MGI Symbol | |||||||||
| EMBL | |||||||||
| GenPept | |||||||||
| RNA Seq Atlas | |||||||||