| ID | Sequence | Length | GC content |
|---|---|---|---|
| AGCGGACUGCGCAUGUGCAGGACCCAGCAGGUCUAGAGCUUUUCUGUGU… | 1753 nt | 0.3930 | |
| GGACUUCGAGCCAUGGCGGUGACGGAAGCGAGCCUGUUGCGCCAGUGCC… | 1703 nt | 0.3928 | |
| GGACUUCGAGCCAUGGCGGUGACGGAAGCGAGCCUGUUGCGCCAGUGCC… | 1718 nt | 0.3929 | |
| GGACUUCGAGCCAUGGCGGUGACGGAAGCGAGCCUGUUGCGCCAGUGCC… | 1658 nt | 0.3926 |
This gene encodes a ubiquitin ligase that is a member of the Fanconi anemia complementation group (FANC). Members of this group are related by their assembly into a common nuclear protein complex rather than by sequence similarity. This gene encodes the protein for complementation group L that mediates monoubiquitination of FANCD2 as well as FANCI. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2018] CIViC Summary for FANCL Gene
A study in humans demonstrated that the FANCL gene was upregulated in subcutaneous adipose tissue during short-term weight loss in obese participants [Bollepalli et al. DOI:10.1038/ijo.2017.245].