underfolded helix Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Underdevelopment of the helix that either affects the entire helix, or is localized. (Human Phenotype Ontology, HP_0008577)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008577
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1 genes associated with the underfolded helix phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
SLC6A8 solute carrier family 6 (neurotransmitter transporter), member 8