abnormality of the radial head Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003995
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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