abnormality of the lumbar spine Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the lumbar vertebral column. (Human Phenotype Ontology, HP_0100712)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100712
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Genes

11 genes associated with the abnormality of the lumbar spine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AMER1 APC membrane recruitment protein 1
BMPER BMP binding endothelial regulator
COL2A1 collagen, type II, alpha 1
FGFR3 fibroblast growth factor receptor 3
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
NPR2 natriuretic peptide receptor 2
RPS6KA3 ribosomal protein S6 kinase, 90kDa, polypeptide 3
SC5D sterol-C5-desaturase