Meningioma Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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://ctdbase.org/detail.go?type=disease&acc=MESH:D008579
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Genes

11 genes/proteins associated with the disease Meningioma from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
HES1 hes family bHLH transcription factor 1 2.88009
PTEN phosphatase and tensin homolog 2.88009
MLLT10 myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 10 2.88009
AKT1 v-akt murine thymoma viral oncogene homolog 1 2.88009
NF2 neurofibromin 2 (merlin) 2.88009
SMO smoothened, frizzled class receptor 2.88009
CSTB cystatin B (stefin B) 2.88009
ALAD aminolevulinate dehydratase 2.88009
CTSL cathepsin L 2.88009
PGR progesterone receptor 2.88009
CST3 cystatin C 2.88009