premature ovarian failure Gene Set
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
|
