ovarian failure, premature Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Similar Terms
Downloads & Tools

Genes

24 genes associated with the disease ovarian failure, premature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ACSL6 acyl-CoA synthetase long-chain family member 6
ADAMTS19 ADAM metallopeptidase with thrombospondin type 1 motif, 19
AR androgen receptor
BBS9 Bardet-Biedl syndrome 9
BDNF brain-derived neurotrophic factor
CXCL12 chemokine (C-X-C motif) ligand 12
DMC1 DNA meiotic recombinase 1
FMR1 fragile X mental retardation 1
FSHR follicle stimulating hormone receptor
GPR3 G protein-coupled receptor 3
GSTM1 glutathione S-transferase mu 1
GSTT1 glutathione S-transferase theta 1
INHA inhibin, alpha
LHCGR luteinizing hormone/choriogonadotropin receptor
LHX8 LIM homeobox 8
MSH4 mutS homolog 4
MSH5 mutS homolog 5
NAT2 N-acetyltransferase 2 (arylamine N-acetyltransferase)
NOBOX NOBOX oogenesis homeobox
PCMT1 protein-L-isoaspartate (D-aspartate) O-methyltransferase
PTEN phosphatase and tensin homolog
SPO11 SPO11 meiotic protein covalently bound to DSB
TAF4B TAF4b RNA polymerase II, TATA box binding protein (TBP)-associated factor, 105kDa
USP9X ubiquitin specific peptidase 9, X-linked