aplasia/hypoplasia of the scapulae Gene Set
Genes
18 genes associated with the aplasia/hypoplasia of the scapulae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ACTB
|
actin, beta
|
|
COL11A1
|
collagen, type XI, alpha 1
|
|
DYM
|
dymeclin
|
|
FGFR1
|
fibroblast growth factor receptor 1
|
|
FGFR3
|
fibroblast growth factor receptor 3
|
|
FLNA
|
filamin A, alpha
|
|
GNPTAB
|
N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
|
|
GSC
|
goosecoid homeobox
|
|
NSDHL
|
NAD(P) dependent steroid dehydrogenase-like
|
|
PCNT
|
pericentrin
|
|
RIPK4
|
receptor-interacting serine-threonine kinase 4
|
|
RUNX2
|
runt-related transcription factor 2
|
|
SLC35D1
|
solute carrier family 35 (UDP-GlcA/UDP-GalNAc transporter), member D1
|
|
SOX9
|
SRY (sex determining region Y)-box 9
|
|
TBX15
|
T-box 15
|
|
TBX3
|
T-box 3
|
|
TRIP11
|
thyroid hormone receptor interactor 11
|
|
WDR35
|
WD repeat domain 35
|
