Hyperpigmentation Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description excess of pigment in any or all tissues or a part of a tissue (Mammalian Phenotype Ontology, MP_0001188)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D017495
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Genes

6 genes/proteins associated with the disease Hyperpigmentation from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SLC29A3 solute carrier family 29 (equilibrative nucleoside transporter), member 3 2.88009
RPL27A ribosomal protein L27a 2.88009
DCT dopachrome tautomerase 1.11673
VEGFA vascular endothelial growth factor A 1.09332
CDKN2A cyclin-dependent kinase inhibitor 2A 1.04201
MYB v-myb avian myeloblastosis viral oncogene homolog 1.03197