abnormality of the subungual region Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A lesion located beneath a fingernail or toenail. (Human Phenotype Ontology, HP_0009723)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009723
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7 genes associated with the abnormality of the subungual region 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
CARD14 caspase recruitment domain family, member 14
KRT17 keratin 17, type I
MBTPS2 membrane-bound transcription factor peptidase, site 2
TRPV3 transient receptor potential cation channel, subfamily V, member 3
TSC1 tuberous sclerosis 1
TSC2 tuberous sclerosis 2