decreased fertility Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000144
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Genes

83 genes associated with the decreased fertility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
ALMS1 Alstrom syndrome protein 1
AMH anti-Mullerian hormone
AMHR2 anti-Mullerian hormone receptor, type II
ANOS1 anosmin 1
AR androgen receptor
AURKC aurora kinase C
BLM Bloom syndrome, RecQ helicase-like
BMP15 bone morphogenetic protein 15
BRAF B-Raf proto-oncogene, serine/threonine kinase
BSCL2 Berardinelli-Seip congenital lipodystrophy 2 (seipin)
C21ORF59 chromosome 21 open reading frame 59
CATSPER1 cation channel, sperm associated 1
CCDC39 coiled-coil domain containing 39
CCDC40 coiled-coil domain containing 40
CCDC8 coiled-coil domain containing 8
CCNO cyclin O
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CHD7 chromodomain helicase DNA binding protein 7
CHRM3 cholinergic receptor, muscarinic 3
CTNS cystinosin, lysosomal cystine transporter
CUL7 cullin 7
CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1
DNAAF1 dynein, axonemal, assembly factor 1
DNAAF3 dynein, axonemal, assembly factor 3
DNAAF5 dynein, axonemal, assembly factor 5
DNAI1 dynein, axonemal, intermediate chain 1
DNAI2 dynein, axonemal, intermediate chain 2
DUSP6 dual specificity phosphatase 6
DYX1C1 dyslexia susceptibility 1 candidate 1
FEZF1 FEZ family zinc finger 1
FGF17 fibroblast growth factor 17
FGF8 fibroblast growth factor 8 (androgen-induced)
FGFR1 fibroblast growth factor receptor 1
FLRT3 fibronectin leucine rich transmembrane protein 3
FOXL2 forkhead box L2
FSHR follicle stimulating hormone receptor
GALT galactose-1-phosphate uridylyltransferase
GBA2 glucosidase, beta (bile acid) 2
GOPC golgi-associated PDZ and coiled-coil motif containing
H6PD hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase)
HESX1 HESX homeobox 1
HS6ST1 heparan sulfate 6-O-sulfotransferase 1
HSD17B3 hydroxysteroid (17-beta) dehydrogenase 3
IL17RD interleukin 17 receptor D
KISS1R KISS1 receptor
KLHL10 kelch-like family member 10
LHB luteinizing hormone beta polypeptide
LHCGR luteinizing hormone/choriogonadotropin receptor
MPLKIP M-phase specific PLK1 interacting protein
NANOS1 nanos homolog 1 (Drosophila)
NDN necdin, melanoma antigen (MAGE) family member
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
OBSL1 obscurin-like 1
PGR progesterone receptor
PNPLA6 patatin-like phospholipase domain containing 6
PRLR prolactin receptor
PROK2 prokineticin 2
PROKR2 prokineticin receptor 2
PSMC3IP PSMC3 interacting protein
PTPN11 protein tyrosine phosphatase, non-receptor type 11
RAF1 Raf-1 proto-oncogene, serine/threonine kinase
RNF216 ring finger protein 216
RSPH1 radial spoke head 1 homolog (Chlamydomonas)
SEMA3A sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A
SEPT12 septin 12
SNRPN small nuclear ribonucleoprotein polypeptide N
SOX10 SRY (sex determining region Y)-box 10
SOX9 SRY (sex determining region Y)-box 9
SPATA16 spermatogenesis associated 16
SPRY4 sprouty homolog 4 (Drosophila)
SRD5A2 steroid-5-alpha-reductase, alpha polypeptide 2 (3-oxo-5 alpha-steroid delta 4-dehydrogenase alpha 2)
SRY sex determining region Y
STUB1 STIP1 homology and U-box containing protein 1, E3 ubiquitin protein ligase
TACR3 tachykinin receptor 3
TBX3 T-box 3
TNXB tenascin XB
WDR11 WD repeat domain 11
WRN Werner syndrome, RecQ helicase-like
ZMYND10 zinc finger, MYND-type containing 10
ZP1 zona pellucida glycoprotein 1 (sperm receptor)