delayed eruption of permanent teeth Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Delayed tooth eruption affecting the secondary dentition. (Human Phenotype Ontology, HP_0000696)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000696
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Genes

7 genes associated with the delayed eruption of permanent teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CTSK cathepsin K
FAM20A family with sequence similarity 20, member A
GJA1 gap junction protein, alpha 1, 43kDa
KCNJ2 potassium channel, inwardly rectifying subfamily J, member 2
ROR2 receptor tyrosine kinase-like orphan receptor 2
RUNX2 runt-related transcription factor 2
SMARCB1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1