premature loss of primary teeth Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Loss of the primary (also known as deciduous) teeth before the usual age. (Human Phenotype Ontology, HP_0006323)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006323
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Genes

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

Symbol Name
ALPL alkaline phosphatase, liver/bone/kidney
CLCN7 chloride channel, voltage-sensitive 7
COL3A1 collagen, type III, alpha 1
CTSC cathepsin C
EDAR ectodysplasin A receptor
EDARADD EDAR-associated death domain
FERMT1 fermitin family member 1
FIG4 FIG4 phosphoinositide 5-phosphatase
GJA1 gap junction protein, alpha 1, 43kDa
SNX10 sorting nexin 10
TCIRG1 T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3
TNFSF11 tumor necrosis factor (ligand) superfamily, member 11
TRAF6 TNF receptor-associated factor 6, E3 ubiquitin protein ligase
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor
WNT10A wingless-type MMTV integration site family, member 10A