abnormality of the radial head Gene Set
Genes
21 genes associated with the abnormality of the radial head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Symbol |
Name |
ASXL1
|
additional sex combs like transcriptional regulator 1
|
ATR
|
ATR serine/threonine kinase
|
B3GALT6
|
UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6
|
CD96
|
CD96 molecule
|
CHRNG
|
cholinergic receptor, nicotinic, gamma (muscle)
|
COL27A1
|
collagen, type XXVII, alpha 1
|
CREBBP
|
CREB binding protein
|
ERCC1
|
excision repair cross-complementation group 1
|
FLNA
|
filamin A, alpha
|
GPC6
|
glypican 6
|
GSC
|
goosecoid homeobox
|
IFITM5
|
interferon induced transmembrane protein 5
|
KIF22
|
kinesin family member 22
|
LMX1B
|
LIM homeobox transcription factor 1, beta
|
NIPBL
|
Nipped-B homolog (Drosophila)
|
NOG
|
noggin
|
NOTCH2
|
notch 2
|
PRKAR1A
|
protein kinase, cAMP-dependent, regulatory, type I, alpha
|
SCARF2
|
scavenger receptor class F, member 2
|
SKI
|
SKI proto-oncogene
|
TBX15
|
T-box 15
|