SLX4 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human SLX4 wild-type allele is located in the vicinity of 16p13.3 and is approximately 30 kb in length. This allele, which encodes structure-specific endonuclease subunit SLX4 protein, plays a role in both the regulation of endonuclease activity and the recognition of damaged DNA. Mutation of the gene is associated with Fanconi anemia complementation group P.

**Synonyms:** - BTB (POZ) Domain Containing 12 Gene - BTBD12 - FANCP - Fanconi Anemia, Complementation Group P Gene - KIAA1784 - KIAA1987 - MUS312 - MUS312, Drosophila, Homolog of Gene - SLX4 Structure-Specific Endonuclease Subunit Homolog (S. cerevisiae) Gene - SLX4 Structure-Specific Endonuclease Subunit wt Allele - SLX4, S. cerevisiae, Homolog of Gene