GTF2I
Lua error in Module:Infobox_gene at line 33: attempt to index field 'wikibase' (a nil value). General transcription factor II-I is a protein that in humans is encoded by the GTF2I gene.[1][2][3]
Function
This gene encodes a multifunctional phosphoprotein with roles in transcription and signal transduction. It is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23. The exon(s) encoding 5' UTR has not been fully defined, but this gene is known to contain at least 34 exons, and its alternative splicing generates 4 transcript variants.[3]
Interactions
GTF2I has been shown to interact with:
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References
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External links
- GTF2I protein, human at the US National Library of Medicine Medical Subject Headings (MeSH)
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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