abnormality of the axillary hair Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	Abnormality of the growth of the axillary hair. Axillary hair is part of the secondary sexual hair, which normally ensues during puberty. (Human Phenotype Ontology, HP_0100134)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0100134
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Genes

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

Symbol	Name
APOE	apolipoprotein E
AR	androgen receptor
DSC3	desmocollin 3
GJB6	gap junction protein, beta 6, 30kDa
LPAR6	lysophosphatidic acid receptor 6
MAP3K1	mitogen-activated protein kinase kinase kinase 1, E3 ubiquitin protein ligase
SNRPE	small nuclear ribonucleoprotein polypeptide E
TBX3	T-box 3
TP63	tumor protein p63
ZBTB20	zinc finger and BTB domain containing 20