meningioma Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A central nervous system cancer that are manifested in the central nervous system and arise from the arachnoid cap cells of the arachnoid villi in the meninges. (Human Disease Ontology, DOID_3565)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002858
Similar Terms
Downloads & Tools

Genes

17 genes associated with the meningioma 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
ARMC5 armadillo repeat containing 5
BAP1 BRCA1 associated protein-1 (ubiquitin carboxy-terminal hydrolase)
CHEK2 checkpoint kinase 2
KLLN killin, p53-regulated DNA replication inhibitor
MN1 meningioma (disrupted in balanced translocation) 1
NF1 neurofibromin 1
NF2 neurofibromin 2 (merlin)
NRAS neuroblastoma RAS viral (v-ras) oncogene homolog
PDGFB platelet-derived growth factor beta polypeptide
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
PTCH1 patched 1
PTEN phosphatase and tensin homolog
SDHB succinate dehydrogenase complex, subunit B, iron sulfur (Ip)
SDHC succinate dehydrogenase complex, subunit C, integral membrane protein, 15kDa
SDHD succinate dehydrogenase complex, subunit D, integral membrane protein
WRN Werner syndrome, RecQ helicase-like