abnormality of the thoracic spine Gene Set
Genes
18 genes associated with the abnormality of the thoracic spine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ALDH3A2
|
aldehyde dehydrogenase 3 family, member A2
|
|
AMER1
|
APC membrane recruitment protein 1
|
|
ANKRD11
|
ankyrin repeat domain 11
|
|
COL2A1
|
collagen, type II, alpha 1
|
|
DYM
|
dymeclin
|
|
GNPTAB
|
N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
|
|
GUSB
|
glucuronidase, beta
|
|
MAN2B1
|
mannosidase, alpha, class 2B, member 1
|
|
MGAT2
|
mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase
|
|
MOGS
|
mannosyl-oligosaccharide glucosidase
|
|
NPR2
|
natriuretic peptide receptor 2
|
|
PIK3R2
|
phosphoinositide-3-kinase, regulatory subunit 2 (beta)
|
|
RBBP8
|
retinoblastoma binding protein 8
|
|
SMARCAL1
|
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a-like 1
|
|
SRD5A3
|
steroid 5 alpha-reductase 3
|
|
TBX5
|
T-box 5
|
|
VPS13B
|
vacuolar protein sorting 13 homolog B (yeast)
|
|
WDR81
|
WD repeat domain 81
|
