Reticulate Acropigmentation Of Kitamura Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A pigmentation disease characterized by lesions that initially arise as letiginous, hyperpigmented macules in a reticular pattern on the dorsal aspect of the hands and feet. Over time, lesions may spread proximally and may darken; palmoplantar pitting and dermatoglyphic disruption may also be present. (Human Disease Ontology, DOID_0060258)
External Link https://www.disgenet.org/browser/0/1/0/C0406811
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Genes

5 genes associated with the disease Reticulate Acropigmentation Of Kitamura in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADAM10 ADAM metallopeptidase domain 10
ADAR adenosine deaminase, RNA-specific
KRT5 keratin 5, type II
POFUT1 protein O-fucosyltransferase 1
POGLUT1 protein O-glucosyltransferase 1