abnormality of nail color Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly of the color of the nail. (Human Phenotype Ontology, HP_0100643)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100643
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11 genes associated with the abnormality of nail color phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCA12 ATP-binding cassette, sub-family A (ABC1), member 12
GJB2 gap junction protein, beta 2, 26kDa
GJB6 gap junction protein, beta 6, 30kDa
KIF11 kinesin family member 11
KRT16 keratin 16, type I
KRT17 keratin 17, type I
KRT6A keratin 6A, type II
KRT6B keratin 6B, type II
PLCD1 phospholipase C, delta 1
STK11 serine/threonine kinase 11
TRPS1 trichorhinophalangeal syndrome I