Health Conditions Related to Genetic Changes
Dowling-Degos disease
At least 13 mutations in the POFUT1 gene have been found to cause Dowling-Degos disease. This condition results in various skin abnormalities, including a characteristic lacy pattern of abnormally dark skin coloring (hyperpigmentation) that occurs most often in the body's folds and creases.
The POFUT1 gene mutations that cause Dowling-Degos disease either lead to an abnormally short protein with no function or change single protein building blocks (amino acids), resulting in a partial loss of protein function. As a result, protein O-fucosyltransferase 1 is less able or unable to add fucose molecules to Notch receptors. Without these sugar molecules, Notch receptors cannot bind to their ligands and the Notch pathway is halted. Because the varied functions of the Notch pathway affect many body systems and Dowling-Degos disease affects only the skin, it is unclear whether the signs and symptoms of this condition are due to impaired Notch signaling or disruption of an unknown function of protein O-fucosyltransferase 1 in melanocytes or other skin cells.
More About This Health ConditionOther Names for This Gene
- FUT12
- KIAA0180
- O-Fuc-T
- o-fucosyltransferase protein
- O-FucT-1
- O-FUT
- OFUCT1
- peptide-O-fucosyltransferase 1
Additional Information & Resources
Tests Listed in the Genetic Testing Registry
Scientific Articles on PubMed
Catalog of Genes and Diseases from OMIM
References
- Buket Basmanav F, Fritz G, Lestringant GG, Pachat D, Hoffjan S, Fischer J, Wehner M, Wolf S, Thiele H, Altmuller J, Pulimood SA, Rutten A, Kruse R, Hanneken S, Frank J, Danda S, Bygum A, Betz RC. Pathogenicity of POFUT1 in Dowling-Degos disease: additional mutations and clinical overlap with reticulate acropigmentation of kitamura. J Invest Dermatol. 2015 Feb;135(2):615-618. doi: 10.1038/jid.2014.406. Epub 2014 Sep 17. No abstract available. Citation on PubMed
- Li M, Cheng R, Liang J, Yan H, Zhang H, Yang L, Li C, Jiao Q, Lu Z, He J, Ji J, Shen Z, Li C, Hao F, Yu H, Yao Z. Mutations in POFUT1, encoding protein O-fucosyltransferase 1, cause generalized Dowling-Degos disease. Am J Hum Genet. 2013 Jun 6;92(6):895-903. doi: 10.1016/j.ajhg.2013.04.022. Epub 2013 May 16. Erratum In: Am J Hum Genet. 2013 Jun 6;92(6):1014. Citation on PubMed or Free article on PubMed Central
- McMillan BJ, Zimmerman B, Egan ED, Lofgren M, Xu X, Hesser A, Blacklow SC. Structure of human POFUT1, its requirement in ligand-independent oncogenic Notch signaling, and functional effects of Dowling-Degos mutations. Glycobiology. 2017 Aug 1;27(8):777-786. doi: 10.1093/glycob/cwx020. Citation on PubMed
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