palpebral edema Gene Set
Genes
17 genes associated with the palpebral edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ABCC9
|
ATP-binding cassette, sub-family C (CFTR/MRP), member 9
|
|
ABCD3
|
ATP-binding cassette, sub-family D (ALD), member 3
|
|
ACTB
|
actin, beta
|
|
ACTG1
|
actin gamma 1
|
|
ADAMTS2
|
ADAM metallopeptidase with thrombospondin type 1 motif, 2
|
|
AIP
|
aryl hydrocarbon receptor interacting protein
|
|
ANTXR1
|
anthrax toxin receptor 1
|
|
CAMTA1
|
calmodulin binding transcription activator 1
|
|
DUX4
|
double homeobox 4
|
|
FOXG1
|
forkhead box G1
|
|
FRG1
|
FSHD region gene 1
|
|
GNPTAB
|
N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
|
|
KCTD1
|
potassium channel tetramerization domain containing 1
|
|
PEX5
|
peroxisomal biogenesis factor 5
|
|
RIN2
|
Ras and Rab interactor 2
|
|
SHANK3
|
SH3 and multiple ankyrin repeat domains 3
|
|
SMCHD1
|
structural maintenance of chromosomes flexible hinge domain containing 1
|
