Premature Ovarian Failure Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An ovarian disease where ovaries do not produce estrogen despite high levels of circulating gonadotropins in women under 40. (Human Disease Ontology, DOID_5426)
External Link https://www.disgenet.org/browser/0/1/0/C1837008
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Genes

23 genes associated with the disease Premature Ovarian Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
BMP15 bone morphogenetic protein 15
CYP2C19 cytochrome P450, family 2, subfamily C, polypeptide 19
CYP2E1 cytochrome P450, family 2, subfamily E, polypeptide 1
DIAPH2 diaphanous-related formin 2
ERCC6 excision repair cross-complementation group 6
FANCM Fanconi anemia, complementation group M
FIGLA folliculogenesis specific basic helix-loop-helix
FMR1 fragile X mental retardation 1
FOXL2 forkhead box L2
GDF9 growth differentiation factor 9
HFM1 HFM1, ATP-dependent DNA helicase homolog (S. cerevisiae)
MCM8 minichromosome maintenance complex component 8
MCM9 minichromosome maintenance complex component 9
MSH5 mutS homolog 5
NFE2L2 nuclear factor, erythroid 2-like 2
NOBOX NOBOX oogenesis homeobox
NR5A1 nuclear receptor subfamily 5, group A, member 1
POF1B premature ovarian failure, 1B
STAG3 stromal antigen 3
SYCE1 synaptonemal complex central element protein 1
WT1 Wilms tumor 1
XPNPEP2 X-prolyl aminopeptidase (aminopeptidase P) 2, membrane-bound