Fibroadenoma Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A breast benign neoplasm comprised of fibrous and glandoular tissues located_in breast. (Human Disease Ontology, DOID_1618)
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Genes

14 genes associated with the Fibroadenoma phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
AR androgen receptor
COMT catechol-O-methyltransferase
CYP17A1 cytochrome P450, family 17, subfamily A, polypeptide 1
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
CYP1A1 cytochrome P450, family 1, subfamily A, polypeptide 1
EGFR epidermal growth factor receptor
ERBB2 erb-b2 receptor tyrosine kinase 2
HSD17B1 hydroxysteroid (17-beta) dehydrogenase 1
MED12 mediator complex subunit 12
PRL prolactin
PRLR prolactin receptor
RASSF1 Ras association (RalGDS/AF-6) domain family member 1
SRD5A2 steroid-5-alpha-reductase, alpha polypeptide 2 (3-oxo-5 alpha-steroid delta 4-dehydrogenase alpha 2)
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor