sparse axillary hair Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Reduced number or density of axillary hair. (Human Phenotype Ontology, HP_0002215)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002215
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Genes

6 genes associated with the sparse axillary hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AR androgen receptor
DSC3 desmocollin 3
LPAR6 lysophosphatidic acid receptor 6
MAP3K1 mitogen-activated protein kinase kinase kinase 1, E3 ubiquitin protein ligase
TBX3 T-box 3
TP63 tumor protein p63