TFIIH p89 Monoclonal Antibody, 100ul Pipette Filler Mutations in DRD4 have been

Mutations in DRD4 have been associated with various behavioral phenotypes

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Belongs to the WD repeat BOP1/ERB1 family

The protein encoded by this gene belongs to the G-protein coupled receptor 1 family

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TFIIH p89 Monoclonal Antibody, 100ul Pipette Filler Mutations in DRD4 have beenThis gene encodes an ATP dependent DNA helicase that functions in nucleotide excision repair. The encoded protein is a subunit of basal transcription factor 2 (TFIIH) and, therefore, also functions in class II transcription. Mutations in this gene are associated with Xeroderma pigmentosum B, Cockayne's syndrome, and trichothiodystrophy. Alternative splicing results in multiple transcript variants.