amelogenesis imperfecta Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A dental enamel hypoplasia characterized by abnormal enamel formation. (Human Disease Ontology, DOID_2187)
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12 genes involed in the disease amelogenesis imperfecta from the DISEASES Curated Gene-Disease Assocation Evidence Scores 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
MMP20 matrix metallopeptidase 20
ROGDI rogdi homolog (Drosophila)
SLC24A4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4
STIM1 stromal interaction molecule 1