embryonal neoplasm Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A germ cell cancer that is associated with an embryo. (Human Disease Ontology, DOID_688)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002898
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Genes

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

Symbol Name
APC adenomatous polyposis coli
BRCA2 breast cancer 2, early onset
BUB1 BUB1 mitotic checkpoint serine/threonine kinase
BUB1B BUB1 mitotic checkpoint serine/threonine kinase B
BUB3 BUB3 mitotic checkpoint protein
CDC73 cell division cycle 73
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
CEP57 centrosomal protein 57kDa
CHEK2 checkpoint kinase 2
DIS3L2 DIS3 like 3'-5' exoribonuclease 2
FGFR3 fibroblast growth factor receptor 3
GPC3 glypican 3
GPC4 glypican 4
H19 H19, imprinted maternally expressed transcript (non-protein coding)
HDAC4 histone deacetylase 4
IGF2 insulin-like growth factor 2
KCNQ1OT1 KCNQ1 opposite strand/antisense transcript 1 (non-protein coding)
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
MNX1 motor neuron and pancreas homeobox 1
NFIX nuclear factor I/X (CCAAT-binding transcription factor)
NSD1 nuclear receptor binding SET domain protein 1
PALB2 partner and localizer of BRCA2
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
RB1 retinoblastoma 1
SETBP1 SET binding protein 1
SLC22A18 solute carrier family 22, member 18
SLC37A4 solute carrier family 37 (glucose-6-phosphate transporter), member 4
STK11 serine/threonine kinase 11
TP53 tumor protein p53
TRIM37 tripartite motif containing 37
WT1 Wilms tumor 1