Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10919
Gene Symbol: EHMT2
EHMT2
0.300 Biomarker phenotype CTD_human Pubertal exposure to di-(2-ethylhexyl)-phthalate inhibits G9a-mediated histone methylation during spermatogenesis in mice. 25975992 2016
Entrez Id: 54902
Gene Symbol: TTC19
TTC19
0.300 Biomarker phenotype CTD_human Mutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and flies. 21278747 2011
Entrez Id: 3953
Gene Symbol: LEPR
LEPR
0.300 Biomarker phenotype CTD_human Neuropeptidergic characterization of the leptin receptor mutated obese Koletsky rat. 15093691 2004
Entrez Id: 5732
Gene Symbol: PTGER2
PTGER2
0.300 Biomarker phenotype CTD_human Using mice deficient in 1 of 4 prostaglandin E2 (PGE2) receptors -- specifically, the EP2 receptor -- we show that Ep2(-/-) females are infertile secondary to failure of the released ovum to become fertilized in vivo. 10359563 1999
Entrez Id: 9365
Gene Symbol: KL
KL
0.300 Biomarker phenotype CTD_human A defect in klotho gene expression in the mouse results in a syndrome that resembles human ageing, including a short lifespan, infertility, arteriosclerosis, skin atrophy, osteoporosis and emphysema. 9363890 1997
Entrez Id: 472
Gene Symbol: ATM
ATM
0.200 Biomarker phenotype RGD Rats with a missense mutation in Atm display neuroinflammation and neurodegeneration subsequent to accumulation of cytosolic DNA following unrepaired DNA damage. 27895165 2017
Entrez Id: 472
Gene Symbol: ATM
ATM
0.200 Biomarker phenotype RGD A rat model of ataxia-telangiectasia: evidence for a neurodegenerative phenotype. 28007901 2017
Entrez Id: 2099
Gene Symbol: ESR1
ESR1
0.200 Biomarker phenotype RGD Both male and female Esr1-null rats were infertile. 24506075 2014
Entrez Id: 675
Gene Symbol: BRCA2
BRCA2
0.200 Biomarker phenotype RGD Production of knockout rats using ENU mutagenesis and a yeast-based screening assay. 12754522 2003
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
0.110 Biomarker phenotype LHGDN In these LMNA-linked lipodystrophic patients, the prevalence of PCOS, infertility, and gestational diabetes was higher than in the general population. 18364375 2008
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
0.110 Biomarker phenotype HPO
Entrez Id: 10149
Gene Symbol: ADGRG2
ADGRG2
0.100 CausalMutation phenotype CLINVAR Truncating Mutations in the Adhesion G Protein-Coupled Receptor G2 Gene ADGRG2 Cause an X-Linked Congenital Bilateral Absence of Vas Deferens. 27476656 2016
Entrez Id: 9742
Gene Symbol: IFT140
IFT140
0.100 CausalMutation phenotype CLINVAR Impact of whole exome sequencing among Iranian patients with autosomal recessive retinitis pigmentosa. 26497376 2015
Entrez Id: 83544
Gene Symbol: DNAL1
DNAL1
0.100 Biomarker phenotype HPO
Entrez Id: 54768
Gene Symbol: HYDIN
HYDIN
0.100 Biomarker phenotype HPO
Entrez Id: 140732
Gene Symbol: SUN5
SUN5
0.100 Biomarker phenotype HPO
Entrez Id: 6638
Gene Symbol: SNRPN
SNRPN
0.100 Biomarker phenotype HPO
Entrez Id: 85016
Gene Symbol: CFAP300
CFAP300
0.100 Biomarker phenotype HPO
Entrez Id: 9101
Gene Symbol: USP8
USP8
0.100 Biomarker phenotype HPO
Entrez Id: 353238
Gene Symbol: PADI6
PADI6
0.100 Biomarker phenotype HPO
Entrez Id: 5618
Gene Symbol: PRLR
PRLR
0.100 Biomarker phenotype HPO
Entrez Id: 50846
Gene Symbol: DHH
DHH
0.100 Biomarker phenotype HPO
Entrez Id: 4692
Gene Symbol: NDN
NDN
0.100 Biomarker phenotype HPO
Entrez Id: 23742
Gene Symbol: NPAP1
NPAP1
0.100 Biomarker phenotype HPO
Entrez Id: 6674
Gene Symbol: SPAG1
SPAG1
0.100 Biomarker phenotype HPO