FAM111A wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human FAM111A wild-type allele is located in the vicinity of 11q12.1 and is approximately 12 kb in length. This allele, which encodes serine protease FAM111A protein, plays a role in the repair of DNA-protein crosslinks. Mutations in the gene are associated with both Gracile bone dysplasia and Kenny-Caffey syndrome 2.

**Synonyms:** - FAM111 Trypsin Like Peptidase A wt Allele - FLJ22794 - Family With Sequence Similarity 111 Member A Gene - GCLEB - KCS2 - KIAA1895