spinal cord compression Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description External mechanical compression of the spinal cord. (Human Phenotype Ontology, HP_0002176)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002176
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12 genes associated with the spinal cord compression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AKT1 v-akt murine thymoma viral oncogene homolog 1
B3GALT6 UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6
COMP cartilage oligomeric matrix protein
DDR2 discoidin domain receptor tyrosine kinase 2
DNA2 DNA replication helicase/nuclease 2
FLNB filamin B, beta
IDS iduronate 2-sulfatase
NME1 NME/NM23 nucleoside diphosphate kinase 1
PHEX phosphate regulating endopeptidase homolog, X-linked
RMRP RNA component of mitochondrial RNA processing endoribonuclease
SLC26A2 solute carrier family 26 (anion exchanger), member 2
TRPV4 transient receptor potential cation channel, subfamily V, member 4