persistence of primary teeth Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Persistence of the primary teeth beyond the age by which they normally are shed and replaced by the permanent teeth. (Human Phenotype Ontology, HP_0006335)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006335
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Genes

9 genes associated with the persistence of primary teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BCOR BCL6 corepressor
CTSK cathepsin K
EHMT1 euchromatic histone-lysine N-methyltransferase 1
FLNA filamin A, alpha
KCNJ2 potassium channel, inwardly rectifying subfamily J, member 2
PTH1R parathyroid hormone 1 receptor
RAB23 RAB23, member RAS oncogene family
STAT3 signal transducer and activator of transcription 3 (acute-phase response factor)
TNFSF11 tumor necrosis factor (ligand) superfamily, member 11