amelogenesis imperfecta Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A dental enamel hypoplasia characterized by abnormal enamel formation. (Human Disease Ontology, DOID_2187)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000705
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Genes

14 genes associated with the amelogenesis imperfecta phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AMELX amelogenin, X-linked
C4ORF26 chromosome 4 open reading frame 26
CNNM4 cyclin and CBS domain divalent metal cation transport mediator 4
DLX3 distal-less homeobox 3
ENAM enamelin
FAM20A family with sequence similarity 20, member A
FAM83H family with sequence similarity 83, member H
KLK4 kallikrein-related peptidase 4
LAMA3 laminin, alpha 3
MMP20 matrix metallopeptidase 20
ROGDI rogdi homolog (Drosophila)
SLC24A4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4
TMEM165 transmembrane protein 165
WDR72 WD repeat domain 72