PHF6 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human PHF6 wild-type allele is located in the vicinity of Xq26.2 and is approximately 56 kb in length. This allele, which encodes PHD finger protein 6, is involved in the regulation of transcription. Mutation of the gene is associated with Borjeson-Forssman-Lehmann syndrome.

**Synonyms:** - BFLS - BORJ - Borjeson-Forssman-Lehmann Syndrome Gene - CENP-31 - Centromere Protein 31 Gene - KIAA1823 - MGC14797 - PHD Finger Protein 6 wt Allele