Health Conditions Related to Genetic Changes
Dowling-Degos disease
At least 11 mutations in the POGLUT1 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.
Most of the POGLUT1 gene mutations that cause Dowling-Degos disease 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-glucosyltransferase 1 is less able or unable to add glucose 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-glucosyltransferase 1 in melanocytes or other skin cells.
More About This Health ConditionLimb-girdle muscular dystrophy
MedlinePlus Genetics provides information about Limb-girdle muscular dystrophy
More About This Health ConditionOther Names for This Gene
- C3orf9
- CAP10-like 46 kDa protein
- CLP46
- hCLP46
- hRumi
- KDELC family like 1
- KDELCL1
- KTEL (Lys-Tyr-Glu-Leu) containing 1
- KTEL motif-containing protein 1
- KTELC1
- LGMD2Z
- MDS010
- MGC32995
- O-glucosyltransferase Rumi homolog
- protein O-xylosyltransferase
- Rumi
Additional Information & Resources
Tests Listed in the Genetic Testing Registry
Scientific Articles on PubMed
Catalog of Genes and Diseases from OMIM
References
- Basmanav FB, Oprisoreanu AM, Pasternack SM, Thiele H, Fritz G, Wenzel J, Grosser L, Wehner M, Wolf S, Fagerberg C, Bygum A, Altmuller J, Rutten A, Parmentier L, El Shabrawi-Caelen L, Hafner C, Nurnberg P, Kruse R, Schoch S, Hanneken S, Betz RC. Mutations in POGLUT1, encoding protein O-glucosyltransferase 1, cause autosomal-dominant Dowling-Degos disease. Am J Hum Genet. 2014 Jan 2;94(1):135-43. doi: 10.1016/j.ajhg.2013.12.003. Citation on PubMed or Free article on PubMed Central
- Chen M, Li Y, Liu H, Fu X, Yu Y, Yu G, Wang C, Bao F, Liany H, Wang Z, Shi Z, Zhang D, Zhou G, Liu J, Zhang F. Analysis of POFUT1 gene mutation in a Chinese family with Dowling-Degos disease. PLoS One. 2014 Aug 26;9(8):e104496. doi: 10.1371/journal.pone.0104496. eCollection 2014. Citation on PubMed or Free article on PubMed Central
- Wilson NJ, Cole C, Kroboth K, Hunter WN, Mann JA, McLean WH, Kernland Lang K, Beltraminelli H, Sabroe RA, Tiffin N, Sobey GJ, Borradori L, Simpson E, Smith FJ. Mutations in POGLUT1 in Galli-Galli/Dowling-Degos disease. Br J Dermatol. 2017 Jan;176(1):270-274. doi: 10.1111/bjd.14914. Epub 2016 Sep 24. No abstract available. Citation on PubMed or Free article on PubMed Central
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