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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.
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Protein Aliases: BarH-like 1 homeobox protein; BarH-like homeobox 1; PKCdeltaVIII
Gene Aliases: BARHL1; FKSG31
UniProt ID: (Human) Q9BZE3
Entrez Gene ID: (Human) 56751
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