neuroectodermal neoplasm Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A neoplasm arising in the neuroectoderm, the portion of the ectoderm of the early embryo that gives rise to the central and peripheral nervous systems, including some glial cells. (Human Phenotype Ontology, HP_0030061)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0030061
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Genes

36 genes associated with the neuroectodermal neoplasm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
APC adenomatous polyposis coli
ASCL1 achaete-scute family bHLH transcription factor 1
BDNF brain-derived neurotrophic factor
BRAF B-Raf proto-oncogene, serine/threonine kinase
CDKN2A cyclin-dependent kinase inhibitor 2A
CHEK2 checkpoint kinase 2
EDN3 endothelin 3
ERBB2 erb-b2 receptor tyrosine kinase 2
GABRD gamma-aminobutyric acid (GABA) A receptor, delta
GDNF glial cell derived neurotrophic factor
GPC3 glypican 3
GPC4 glypican 4
H19 H19, imprinted maternally expressed transcript (non-protein coding)
KCNAB2 potassium channel, voltage gated subfamily A regulatory beta subunit 2
MLH1 mutL homolog 1
MSH2 mutS homolog 2
MSH6 mutS homolog 6
NBN nibrin
NF1 neurofibromin 1
NF2 neurofibromin 2 (merlin)
NME1 NME/NM23 nucleoside diphosphate kinase 1
PALB2 partner and localizer of BRCA2
PHOX2B paired-like homeobox 2b
PMS2 PMS2 postmeiotic segregation increased 2 (S. cerevisiae)
PRDM16 PR domain containing 16
PTCH1 patched 1
PTPN11 protein tyrosine phosphatase, non-receptor type 11
RAF1 Raf-1 proto-oncogene, serine/threonine kinase
RB1 retinoblastoma 1
RET ret proto-oncogene
RUNX1 runt-related transcription factor 1
SDHB succinate dehydrogenase complex, subunit B, iron sulfur (Ip)
SKI SKI proto-oncogene
TP53 tumor protein p53
TSC1 tuberous sclerosis 1
TSC2 tuberous sclerosis 2