Breast Diseases Gene Set

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

28 genes associated with the Breast Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
COMT catechol-O-methyltransferase
CYP1B1 cytochrome P450, family 1, subfamily B, polypeptide 1
ERCC2 excision repair cross-complementation group 2
ERCC4 excision repair cross-complementation group 4
ERCC5 excision repair cross-complementation group 5
ESR1 estrogen receptor 1
ESR2 estrogen receptor 2 (ER beta)
HSD17B1 hydroxysteroid (17-beta) dehydrogenase 1
IGF1 insulin-like growth factor 1 (somatomedin C)
IGFBP1 insulin-like growth factor binding protein 1
IGFBP3 insulin-like growth factor binding protein 3
LEPR leptin receptor
LPL lipoprotein lipase
MDM2 MDM2 proto-oncogene, E3 ubiquitin protein ligase
MT-ND2 MTND2
PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
PON1 paraoxonase 1
PON2 paraoxonase 2
PPARG peroxisome proliferator-activated receptor gamma
PPP2R1A protein phosphatase 2, regulatory subunit A, alpha
PPP2R2A protein phosphatase 2, regulatory subunit B, alpha
PPP2R5E protein phosphatase 2, regulatory subunit B', epsilon isoform
RAD23B RAD23 homolog B (S. cerevisiae)
SULT1A1 sulfotransferase family, cytosolic, 1A, phenol-preferring, member 1
TNF tumor necrosis factor
XPC xeroderma pigmentosum, complementation group C
XRCC1 X-ray repair complementing defective repair in Chinese hamster cells 1
XRCC2 X-ray repair complementing defective repair in Chinese hamster cells 2