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BARHL1 (BarH Like Homeobox 1) is a Protein Coding gene. Diseases associated with BARHL1 include Deafness, Autosomal Recessive 27 and Deafness, Autosomal Dominant 16. Gene Ontology (GO) annotations related to this gene include sequence-specific DNA binding and proximal promoter DNA-binding transcription activator activity, RNA polymerase II-specific. An important paralog of this gene is BARHL2.
Bar-class homeodomain protein MBH2; BarH like homeobox 1; BARHL1; Barhl2; BarH-like 1 (Drosophila); barH-like 1 homeobox protein; BarH-like 2; BarH-like homeobox 1; barH-related homeobox protein 1; Bhx1; Dres115; FKSG31; Mbh2; PKCdeltaVIII
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100 µg
100 µg
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50 µg
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