hypoplastic helices Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Underdevelopment of the helix, i.e., of the outer rim of the pinna. (Human Phenotype Ontology, HP_0008589)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008589
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6 genes associated with the hypoplastic helices phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FRAS1 Fraser extracellular matrix complex subunit 1
FREM2 FRAS1 related extracellular matrix protein 2
GNAI3 guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 3
GRIP1 glutamate receptor interacting protein 1
PLCB4 phospholipase C, beta 4
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)