dry hair Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Hair that lacks the lustre (shine or gleam) of normal hair. (Human Phenotype Ontology, HP_0011359)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011359
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9 genes associated with the dry hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ASL argininosuccinate lyase
BCS1L BC1 (ubiquinol-cytochrome c reductase) synthesis-like
ERCC6 excision repair cross-complementation group 6
ERCC8 excision repair cross-complementation group 8
GJA1 gap junction protein, alpha 1, 43kDa
KRT17 keratin 17, type I
KRT74 keratin 74, type II
LPAR6 lysophosphatidic acid receptor 6
WNT10A wingless-type MMTV integration site family, member 10A