abnormality of the menstrual cycle Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the ovulation cycle. (Human Phenotype Ontology, HP_0000140)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000140
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Genes

116 genes associated with the abnormality of the menstrual cycle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AGGF1 angiogenic factor with G patch and FHA domains 1
AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
AIP aryl hydrocarbon receptor interacting protein
ALMS1 Alstrom syndrome protein 1
ANOS1 anosmin 1
ANTXR1 anthrax toxin receptor 1
AR androgen receptor
ARMC5 armadillo repeat containing 5
BMP15 bone morphogenetic protein 15
BMPR1B bone morphogenetic protein receptor, type IB
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
CAV1 caveolin 1, caveolae protein, 22kDa
CHD7 chromodomain helicase DNA binding protein 7
CLPP caseinolytic mitochondrial matrix peptidase proteolytic subunit
CTDP1 CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) phosphatase, subunit 1
CYP17A1 cytochrome P450, family 17, subfamily A, polypeptide 1
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
DHH desert hedgehog
DUSP6 dual specificity phosphatase 6
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
ERCC8 excision repair cross-complementation group 8
ESR1 estrogen receptor 1
F10 coagulation factor X
F2 coagulation factor II (thrombin)
F5 coagulation factor V (proaccelerin, labile factor)
F7 coagulation factor VII (serum prothrombin conversion accelerator)
FEZF1 FEZ family zinc finger 1
FGA fibrinogen alpha chain
FGB fibrinogen beta chain
FGF17 fibroblast growth factor 17
FGF8 fibroblast growth factor 8 (androgen-induced)
FGFR1 fibroblast growth factor receptor 1
FGG fibrinogen gamma chain
FLRT3 fibronectin leucine rich transmembrane protein 3
FMR1 fragile X mental retardation 1
FOS FBJ murine osteosarcoma viral oncogene homolog
FOXL2 forkhead box L2
FSHB follicle stimulating hormone, beta polypeptide
FSHR follicle stimulating hormone receptor
GFI1B growth factor independent 1B transcription repressor
GHR growth hormone receptor
GNAS GNAS complex locus
GNRHR gonadotropin-releasing hormone receptor
GP1BA glycoprotein Ib (platelet), alpha polypeptide
GP1BB glycoprotein Ib (platelet), beta polypeptide
GP6 glycoprotein VI (platelet)
GP9 glycoprotein IX (platelet)
H6PD hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase)
HARS2 histidyl-tRNA synthetase 2, mitochondrial
HDAC8 histone deacetylase 8
HESX1 HESX homeobox 1
HFE hemochromatosis
HFM1 HFM1, ATP-dependent DNA helicase homolog (S. cerevisiae)
HS6ST1 heparan sulfate 6-O-sulfotransferase 1
HSD17B4 hydroxysteroid (17-beta) dehydrogenase 4
IL17RD interleukin 17 receptor D
ITGA2B integrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41)
ITGA8 integrin, alpha 8
ITGB3 integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
KISS1R KISS1 receptor
LARS2 leucyl-tRNA synthetase 2, mitochondrial
LHX4 LIM homeobox 4
LMNA lamin A/C
MCFD2 multiple coagulation factor deficiency 2
MYH9 myosin, heavy chain 9, non-muscle
NBEAL2 neurobeachin-like 2
NDN necdin, melanoma antigen (MAGE) family member
NIN ninein (GSK3B interacting protein)
NIPBL Nipped-B homolog (Drosophila)
NR3C1 nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
NR5A1 nuclear receptor subfamily 5, group A, member 1
NSMF NMDA receptor synaptonuclear signaling and neuronal migration factor
PAPSS2 3'-phosphoadenosine 5'-phosphosulfate synthase 2
PAX2 paired box 2
PCSK1 proprotein convertase subtilisin/kexin type 1
PLAU plasminogen activator, urokinase
PLIN1 perilipin 1
POF1B premature ovarian failure, 1B
POLG polymerase (DNA directed), gamma
PPARG peroxisome proliferator-activated receptor gamma
PPP1R3A protein phosphatase 1, regulatory subunit 3A
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
PRLR prolactin receptor
PROK2 prokineticin 2
PROKR2 prokineticin receptor 2
PSMC3IP PSMC3 interacting protein
PTPN11 protein tyrosine phosphatase, non-receptor type 11
RAD21 RAD21 homolog (S. pombe)
RET ret proto-oncogene
RNF216 ring finger protein 216
SEMA3A sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
SMC1A structural maintenance of chromosomes 1A
SMC3 structural maintenance of chromosomes 3
SNRPN small nuclear ribonucleoprotein polypeptide N
SOX10 SRY (sex determining region Y)-box 10
SPRY4 sprouty homolog 4 (Drosophila)
SRY sex determining region Y
SSTR5 somatostatin receptor 5
STAG3 stromal antigen 3
TAC3 tachykinin 3
TACR3 tachykinin receptor 3
TNXB tenascin XB
TRMT10A tRNA methyltransferase 10 homolog A (S. cerevisiae)
VWF von Willebrand factor
WAS Wiskott-Aldrich syndrome
WDR11 WD repeat domain 11
WIPF1 WAS/WASL interacting protein family, member 1
WNT4 wingless-type MMTV integration site family, member 4
WNT7A wingless-type MMTV integration site family, member 7A
WRN Werner syndrome, RecQ helicase-like
WT1 Wilms tumor 1