premature ovarian failure Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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 http://compbio.charite.de/hpoweb/showterm?id=HP:0008209
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Genes

17 genes associated with the premature ovarian failure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AARS2 alanyl-tRNA synthetase 2, mitochondrial
C10ORF2 chromosome 10 open reading frame 2
DIAPH2 diaphanous-related formin 2
EIF2B1 eukaryotic translation initiation factor 2B, subunit 1 alpha, 26kDa
EIF2B2 eukaryotic translation initiation factor 2B, subunit 2 beta, 39kDa
EIF2B3 eukaryotic translation initiation factor 2B, subunit 3 gamma, 58kDa
EIF2B4 eukaryotic translation initiation factor 2B, subunit 4 delta, 67kDa
EIF2B5 eukaryotic translation initiation factor 2B, subunit 5 epsilon, 82kDa
FIGLA folliculogenesis specific basic helix-loop-helix
FMR1 fragile X mental retardation 1
FOXL2 forkhead box L2
GALT galactose-1-phosphate uridylyltransferase
LARS2 leucyl-tRNA synthetase 2, mitochondrial
NOBOX NOBOX oogenesis homeobox
NR5A1 nuclear receptor subfamily 5, group A, member 1
POF1B premature ovarian failure, 1B
POLG polymerase (DNA directed), gamma