prominent antihelix Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of an abnormally prominent antihelix. (Human Phenotype Ontology, HP_0000395)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000395
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Genes

5 genes associated with the prominent antihelix phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AP4E1 adaptor-related protein complex 4, epsilon 1 subunit
EVC Ellis van Creveld protein
GLI2 GLI family zinc finger 2
RBM10 RNA binding motif protein 10
SLC16A2 solute carrier family 16, member 2 (thyroid hormone transporter)