abnormality of the alveolar ridges Gene Set
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
|
