premature loss of teeth Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Premature loss of teeth not related to trauma or neglect. (Human Phenotype Ontology, HP_0006480)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006480
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Genes

41 genes associated with the premature loss of 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
COX1
COX2
COX3
CTSC cathepsin C
DKC1 dyskeratosis congenita 1, dyskerin
DST dystonin
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
KRT14 keratin 14, type I
LMNA lamin A/C
MT-ND4 NADH dehydrogenase, subunit 4 (complex I)
MT-ND5 NADH dehydrogenase, subunit 5 (complex I)
MT-ND6 NADH dehydrogenase, subunit 6 (complex I)
MT-TF tRNA
MT-TH tRNA
MT-TL1 tRNA
MT-TQ tRNA
MT-TS1 tRNA
MT-TS2 tRNA
MT-TW tRNA
ND1
NOTCH2 notch 2
PHEX phosphate regulating endopeptidase homolog, X-linked
RUNX2 runt-related transcription factor 2
SH3PXD2B SH3 and PX domains 2B
SNX10 sorting nexin 10
TCIRG1 T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3
TERC telomerase RNA component
TNFRSF11B tumor necrosis factor receptor superfamily, member 11b
TNFSF11 tumor necrosis factor (ligand) superfamily, member 11
TP63 tumor protein p63
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
ZMPSTE24 zinc metallopeptidase STE24