FANCG wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human FANCG wild-type allele is located within 9p13 and is approximately 6 kb in length. This allele, which encodes fanconi anemia group G protein, is involved in chromosomal stability and maintenance and DNA interstrand cross-link repair. The allele also plays a putative role in post-replication repair and cell cycle checkpoints. Allelic variants are involved in Fanconi syndrome.

**Synonyms:** - FA Complementation Group G wt Allele - FACG - FAG Gene - Fanconi Anemia Complementation Group G Gene - Fanconi Anemia, Complementation Group G Gene - X-Ray Repair Complementing Defective Repair In Chinese Hamster Cells 9 Gene - X-Ray Repair, Complementing Defective, In Chinese Hamster, 9 Gene - XRCC9