deep plantar creases Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of unusually deep creases (ridges/wrinkles) on the skin of sole of foot. (Human Phenotype Ontology, HP_0001869)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001869
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Genes

7 genes associated with the deep plantar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCC9 ATP-binding cassette, sub-family C (CFTR/MRP), member 9
AIP aryl hydrocarbon receptor interacting protein
ASXL1 additional sex combs like transcriptional regulator 1
CREBBP CREB binding protein
ERCC6 excision repair cross-complementation group 6
HRAS Harvey rat sarcoma viral oncogene homolog
KCNJ8 potassium channel, inwardly rectifying subfamily J, member 8