tooth agenesis Gene Set

Dataset GWASdb SNP-Disease Associations
Category disease or phenotype associations
Type disease
Description A tooth disease characterized by failure to develop on or more missing teeth. (Human Disease Ontology, DOID_0050591)
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21 genes associated with the disease tooth agenesis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

Symbol Name Standardized Value
THSD7B thrombospondin, type I, domain containing 7B 0.986376
GRIN2B glutamate receptor, ionotropic, N-methyl D-aspartate 2B 0.920453
MAP3K9 mitogen-activated protein kinase kinase kinase 9 0.905653
DLGAP1 discs, large (Drosophila) homolog-associated protein 1 0.892579
ERBB2 erb-b2 receptor tyrosine kinase 2 0.88034
LUZP2 leucine zipper protein 2 0.869084
AK9 adenylate kinase 9 0.863933
OFCC1 orofacial cleft 1 candidate 1 0.858922
SMTNL2 smoothelin-like 2 0.811614
GRIK4 glutamate receptor, ionotropic, kainate 4 0.772631
DTX3L deltex 3 like, E3 ubiquitin ligase 0.753174
APOLD1 apolipoprotein L domain containing 1 0.74095
ZBTB24 zinc finger and BTB domain containing 24 0.734059
THBS4 thrombospondin 4 0.734059
SAMSN1 SAM domain, SH3 domain and nuclear localization signals 1 0.720532
TBC1D10C TBC1 domain family, member 10C 0.714351
DPYD dihydropyrimidine dehydrogenase 0.70663
P2RX4 purinergic receptor P2X, ligand gated ion channel, 4 0.704784
RBFOX1 RNA binding protein, fox-1 homolog (C. elegans) 1 0.69773
FAM162A family with sequence similarity 162, member A 0.692747
TEAD1 TEA domain family member 1 (SV40 transcriptional enhancer factor) 0.67631