benign neoplasm of the central nervous system Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100835
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Genes

35 genes associated with the benign neoplasm of the central nervous system 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
ALX3 ALX homeobox 3
ARMC5 armadillo repeat containing 5
BAP1 BRCA1 associated protein-1 (ubiquitin carboxy-terminal hydrolase)
CCBE1 collagen and calcium binding EGF domains 1
CHEK2 checkpoint kinase 2
FAT4 FAT atypical cadherin 4
FOXC2 forkhead box C2
GLI3 GLI family zinc finger 3
KLLN killin, p53-regulated DNA replication inhibitor
MLH1 mutL homolog 1
MN1 meningioma (disrupted in balanced translocation) 1
MSH2 mutS homolog 2
MSH6 mutS homolog 6
NF1 neurofibromin 1
NF2 neurofibromin 2 (merlin)
NOTCH3 notch 3
NRAS neuroblastoma RAS viral (v-ras) oncogene homolog
OCRL oculocerebrorenal syndrome of Lowe
OFD1 oral-facial-digital syndrome 1
PDGFB platelet-derived growth factor beta polypeptide
PDGFRB platelet-derived growth factor receptor, beta polypeptide
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
PMS2 PMS2 postmeiotic segregation increased 2 (S. cerevisiae)
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
SOX2 SRY (sex determining region Y)-box 2
TP53 tumor protein p53
TSC1 tuberous sclerosis 1
TSC2 tuberous sclerosis 2
VHL von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase
WRN Werner syndrome, RecQ helicase-like