CFP wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human CFP wild-type allele is located in the vicinity of Xp11.4 and is approximately 6 kb in length. This allele, which encodes properdin protein, is involved in the positive regulation of the alternative complement pathway. Point mutations in the gene are associated with properdin deficiency.

**Synonyms:** - BFD - Complement Factor Properdin wt Allele - PFC - PFD - PROPERDIN - Properdin P Factor, Complement Gene