selective tooth agenesis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A tooth disease characterized by failure to develop on or more missing teeth. (Human Disease Ontology, DOID_0050591)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001592
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Genes

11 genes associated with the selective tooth agenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATR ATR serine/threonine kinase
B3GALTL beta 1,3-galactosyltransferase-like
BLM Bloom syndrome, RecQ helicase-like
CDH3 cadherin 3, type 1, P-cadherin (placental)
EIF4A3 eukaryotic translation initiation factor 4A3
FLNA filamin A, alpha
GJA1 gap junction protein, alpha 1, 43kDa
GLI2 GLI family zinc finger 2
LTBP3 latent transforming growth factor beta binding protein 3
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit
TP63 tumor protein p63