abnormality of the frontal sinuses Gene Set
Genes
12 genes associated with the abnormality of the frontal sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Symbol |
Name |
AGA
|
aspartylglucosaminidase
|
ALX3
|
ALX homeobox 3
|
ATRX
|
alpha thalassemia/mental retardation syndrome X-linked
|
COL11A1
|
collagen, type XI, alpha 1
|
CTSK
|
cathepsin K
|
DLX3
|
distal-less homeobox 3
|
DNAI1
|
dynein, axonemal, intermediate chain 1
|
FLNA
|
filamin A, alpha
|
KCNJ2
|
potassium channel, inwardly rectifying subfamily J, member 2
|
NOTCH2
|
notch 2
|
RUNX2
|
runt-related transcription factor 2
|
TRIM37
|
tripartite motif containing 37
|