Dowling-Degos disease

Summary
Synonym
  • dark dot disease
  • reticular pigment anomaly of flexures
Definition
A pigmentation disease characterized by a reticulate pattern of abnormally dark skin coloring, particularly in the body's folds and creases.
Super Class
pigmentation disease
Related Genes
Displaying all 5 entries
Gene ID Gene Symbol Description Source
176 ACAN aggrecan
1298 COL9A2 collagen type IX alpha 2 chain
1312 COMT catechol-O-methyltransferase
23509 POFUT1 protein O-fucosyltransferase 1
56983 POGLUT1 protein O-glucosyltransferase 1
Displaying all 2 entries
Gene ID Gene Symbol Description Source
140484 Pofut1 protein O-fucosyltransferase 1
224143 Poglut1 protein O-glucosyltransferase 1
Displaying all 2 entries
Gene ID Gene Symbol Description Source
288091 Poglut1 protein O-glucosyltransferase 1
311551 Pofut1 protein O-fucosyltransferase 1
Displaying all 3 entries
Gene ID Gene Symbol Description Source
36564 O-fut1 O-fucosyltransferase 1
42698 CG31139 uncharacterized protein
326122 rumi rumi
Displaying all 2 entries
Gene ID Gene Symbol Description Source
403029 pofut1 protein O-fucosyltransferase 1
641495 poglut1 protein O-glucosyltransferase 1
Displaying all 2 entries
Gene ID Gene Symbol Description Source Organism
398423 pofut1.L protein O-fucosyltransferase 1 L homeolog Xenopus laevis (African clawed frog)
496411 pofut1 protein O-fucosyltransferase 1 Xenopus tropicalis (tropical clawed frog)
Displaying 1 entry
Gene ID Gene Symbol Description Source
180607 pfut-1 GDP-fucose protein O-fucosyltransferase 1
The Human Phenotype Ontology
Displaying entry 21 - 21 of 21 in total
HPO ID HPO Term
HP:0200034 Papule
Displaying all 2 entries
Gene ID Gene Symbol Description
23509 POFUT1 protein O-fucosyltransferase 1
56983 POGLUT1 protein O-glucosyltransferase 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024