Skull Base Chordoma Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A chordoma that is located_in the skull base. (Human Disease Ontology, DOID_4151)
External Link https://www.disgenet.org/browser/0/1/0/C1335975
Similar Terms
Downloads & Tools

Genes

17 genes associated with the disease Skull Base Chordoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CTSK cathepsin K
GSK3B glycogen synthase kinase 3 beta
LGALS3 lectin, galactoside-binding, soluble, 3
LGALS9 lectin, galactoside-binding, soluble, 9
LIF leukemia inhibitory factor
LMX1A LIM homeobox transcription factor 1, alpha
NPIPB15 nuclear pore complex interacting protein family, member B15
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
PIK3CB phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit beta
PIK3CD phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit delta
PIK3CG phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit gamma
SAMD5 sterile alpha motif domain containing 5
SASH1 SAM and SH3 domain containing 1
SMARCB1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1
TBX1 T-box 1
TGFA transforming growth factor, alpha
VEGFA vascular endothelial growth factor A