abnormal sweat homeostasis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the composition of sweat or the levels of its components. (Human Phenotype Ontology, HP_0040127)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0040127
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Genes

4 genes associated with the abnormal sweat homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
FUCA1 fucosidase, alpha-L- 1, tissue
SCNN1A sodium channel, non voltage gated 1 alpha subunit
SCNN1B sodium channel, non voltage gated 1 beta subunit