abnormality of the alveolar ridges Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Any abnormality of the alveolar ridges (on the upper or lower jaws). The alveolar ridges contain the sockets (alveoli) of the teeth. (Human Phenotype Ontology, HP_0006477)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006477
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Genes

18 genes associated with the abnormality of the alveolar ridges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ARX aristaless related homeobox
ASXL1 additional sex combs like transcriptional regulator 1
CD96 CD96 molecule
CTSC cathepsin C
DHCR24 24-dehydrocholesterol reductase
DHCR7 7-dehydrocholesterol reductase
DIS3L2 DIS3 like 3'-5' exoribonuclease 2
EIF4A3 eukaryotic translation initiation factor 4A3
EVC Ellis van Creveld protein
EVC2 Ellis van Creveld syndrome 2
FIG4 FIG4 phosphoinositide 5-phosphatase
GJA1 gap junction protein, alpha 1, 43kDa
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
GPC3 glypican 3
IRF6 interferon regulatory factor 6
OFD1 oral-facial-digital syndrome 1
TBX15 T-box 15
ZC4H2 zinc finger, C4H2 domain containing