ridged nail Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Longitudinal, linear prominences in the nail plate. (Human Phenotype Ontology, HP_0001807)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001807
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Genes

14 genes associated with the ridged nail phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATP2A2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
ATR ATR serine/threonine kinase
CTSK cathepsin K
DKC1 dyskeratosis congenita 1, dyskerin
EFNB1 ephrin-B1
FERMT1 fermitin family member 1
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
KRT14 keratin 14, type I
KRT5 keratin 5, type II
LMX1B LIM homeobox transcription factor 1, beta
LPAR6 lysophosphatidic acid receptor 6
MSX1 msh homeobox 1
TERC telomerase RNA component
WNT10A wingless-type MMTV integration site family, member 10A