abnormality of the thoracic spine Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the thoracic vertebral column. (Human Phenotype Ontology, HP_0100711)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100711
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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