Neoplastic Syndromes, Hereditary Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

35 genes associated with the Neoplastic Syndromes, Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
APC adenomatous polyposis coli
BARD1 BRCA1 associated RING domain 1
BMPR1A bone morphogenetic protein receptor, type IA
BRAF B-Raf proto-oncogene, serine/threonine kinase
BRCA1 breast cancer 1, early onset
BRCA2 breast cancer 2, early onset
CDH1 cadherin 1, type 1, E-cadherin (epithelial)
CHEK2 checkpoint kinase 2
CTCF CCCTC-binding factor (zinc finger protein)
CYLD cylindromatosis (turban tumor syndrome)
FAM175A family with sequence similarity 175, member A
FANCB Fanconi anemia, complementation group B
GEN1 GEN1 Holliday junction 5' flap endonuclease
GSTM1 glutathione S-transferase mu 1
GSTP1 glutathione S-transferase pi 1
GSTT1 glutathione S-transferase theta 1
MAX MYC associated factor X
MLH1 mutL homolog 1
MSH2 mutS homolog 2
MSH6 mutS homolog 6
MUTYH mutY homolog
NF1 neurofibromin 1
PALB2 partner and localizer of BRCA2
PMS2 PMS2 postmeiotic segregation increased 2 (S. cerevisiae)
PTEN phosphatase and tensin homolog
RET ret proto-oncogene
SDHAF2 succinate dehydrogenase complex assembly factor 2
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
SMAD4 SMAD family member 4
STK11 serine/threonine kinase 11
TMEM127 transmembrane protein 127
UIMC1 ubiquitin interaction motif containing 1
VHL von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase