diastema Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Increased space between two adjacent teeth in the same dental arch. (Human Phenotype Ontology, HP_0000699)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000699
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Genes

7 genes associated with the diastema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALX3 ALX homeobox 3
ANKRD11 ankyrin repeat domain 11
ATRX alpha thalassemia/mental retardation syndrome X-linked
CHSY1 chondroitin sulfate synthase 1
KDM5C lysine (K)-specific demethylase 5C
MGAT2 mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase
NHS Nance-Horan syndrome (congenital cataracts and dental anomalies)