Dysmenorrhea Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Pain during menstruation that interferes with daily activities. (Human Phenotype Ontology, HP_0100607)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D004412
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Genes

10 genes/proteins associated with the disease Dysmenorrhea from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
AVP arginine vasopressin 2.88009
OXT oxytocin/neurophysin I prepropeptide 2.88009
UGT2B7 UDP glucuronosyltransferase 2 family, polypeptide B7 1.22242
IL6 interleukin 6 1.15122
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa 1.10282
REN renin 1.07732
UGT1A8 UDP glucuronosyltransferase 1 family, polypeptide A8 1.03345
HPGD hydroxyprostaglandin dehydrogenase 15-(NAD) 1.02971
SLC22A1 solute carrier family 22 (organic cation transporter), member 1 1.02708
MPO myeloperoxidase 1.02522