secondary amenorrhea Gene Set
Genes
19 genes associated with the secondary amenorrhea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol |
Name |
|
ANTXR1
|
anthrax toxin receptor 1
|
|
BMP15
|
bone morphogenetic protein 15
|
|
CLPP
|
caseinolytic mitochondrial matrix peptidase proteolytic subunit
|
|
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
|
|
FMR1
|
fragile X mental retardation 1
|
|
FSHR
|
follicle stimulating hormone receptor
|
|
HARS2
|
histidyl-tRNA synthetase 2, mitochondrial
|
|
HSD17B4
|
hydroxysteroid (17-beta) dehydrogenase 4
|
|
LARS2
|
leucyl-tRNA synthetase 2, mitochondrial
|
|
LMNA
|
lamin A/C
|
|
NR5A1
|
nuclear receptor subfamily 5, group A, member 1
|
|
PAPSS2
|
3'-phosphoadenosine 5'-phosphosulfate synthase 2
|
|
POLG
|
polymerase (DNA directed), gamma
|
|
PSMC3IP
|
PSMC3 interacting protein
|
|
WRN
|
Werner syndrome, RecQ helicase-like
|
