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TCF4 gene

transcription factor 4

Key facts

Official symbol
TCF4
Full name
TCF4
Chromosome
18
Map location
18q21.2
Organism
Homo sapiens
NCBI Gene ID
6925
Also known as
CDG2T, E2-2, FCD2, FECD3, ITF-2, ITF2

Function summary

This gene encodes transcription factor 4, a basic helix-loop-helix transcription factor. The encoded protein recognizes an Ephrussi-box ('E-box') binding site ('CANNTG') - a motif first identified in immunoglobulin enhancers. This gene is broadly expressed, and may play an important role in nervous system development. Defects in this gene are a cause of Pitt-Hopkins syndrome. In addition, an intronic CTG repeat normally numbering 10-37 repeat units can expand to >50 repeat units and cause Fuchs endothelial corneal dystrophy. Multiple alternatively spliced transcript variants that encode different proteins have been described. [provided by RefSeq, Jul 2016].

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Data source: NCBI Gene · alsesAI Gene Library