Abnormality Of The Integument Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An abnormality of the integument, which consists of the skin and the superficial fascia. (Human Phenotype Ontology, HP_0001574)
External Link https://www.disgenet.org/browser/0/1/0/C4025761
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Genes

3 genes associated with the disease Abnormality Of The Integument in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
GJB2 gap junction protein, beta 2, 26kDa
RET ret proto-oncogene
SLC35C1 solute carrier family 35 (GDP-fucose transporter), member C1