×
Entrez Id:
2488
Gene Symbol:
FSHB
FSHB
0.300
Biomarker
phenotype
CTD_human
Endocrinology of male infertility.
387166
1979
×
Entrez Id:
3972
Gene Symbol:
LHB
LHB
0.300
Biomarker
phenotype
CTD_human
Endocrinology of male infertility.
387166
1979
×
Entrez Id:
3237
Gene Symbol:
HOXD11
HOXD11
0.300
Biomarker
phenotype
CTD_human
Axial homeosis and appendicular skeleton defects in mice with a targeted disruption of hoxd-11.
7925020
1994
×
Entrez Id:
1636
Gene Symbol:
ACE
ACE
0.300
Biomarker
phenotype
CTD_human
Mice lacking angiotensin-converting enzyme have low blood pressure, renal pathology, and reduced male fertility.
8642790
1996
×
Entrez Id:
3972
Gene Symbol:
LHB
LHB
0.300
Biomarker
phenotype
CTD_human
Association of molecular variants of luteinizing hormone with male infertility.
10739843
2000
×
Entrez Id:
1618
Gene Symbol:
DAZL
DAZL
0.010
Biomarker
phenotype
BEFREE
To study the role of the autosomal candidate gene DAZLA (Deleted in AZoospermia Like Autosome) in male subfertility .
11499325
2001
×
Entrez Id:
367
Gene Symbol:
AR
AR
0.320
Biomarker
phenotype
CTD_human
Genotyping of Israeli infertile men with idiopathic oligozoospermia.
12220434
2002
×
Entrez Id:
367
Gene Symbol:
AR
AR
0.320
Biomarker
phenotype
BEFREE
In this study we investigated the association of male subfertility with the length of CAG repeats in the androgen receptor .
11792931
2002
×
Entrez Id:
5887
Gene Symbol:
RAD23B
RAD23B
0.300
Biomarker
phenotype
CTD_human
Developmental defects and male sterility in mice lacking the ubiquitin-like DNA repair gene mHR23B.
11809813
2002
×
Entrez Id:
3972
Gene Symbol:
LHB
LHB
0.300
Biomarker
phenotype
CTD_human
Hypogonadism in a patient with a mutation in the luteinizing hormone beta-subunit gene.
15602022
2004
×
Entrez Id:
1760
Gene Symbol:
DMPK
DMPK
0.010
GeneticVariation
phenotype
BEFREE
The number of CTG repeats in the normal or mutational range of DM1PK gene is associated with neither idiopathic male subfertility nor with clinical characteristics of male subfertility .
15284213
2004
×
Entrez Id:
1586
Gene Symbol:
CYP17A1
CYP17A1
0.300
Biomarker
phenotype
CTD_human
Haploinsufficiency of cytochrome P450 17alpha-hydroxylase/17,20 lyase (CYP17) causes infertility in male mice.
15890676
2005
×
Entrez Id:
867
Gene Symbol:
CBL
CBL
0.300
Biomarker
phenotype
CTD_human
Androgen-dependent apoptosis in male germ cells is regulated through the proto-oncoprotein Cbl.
16301331
2005
×
Entrez Id:
4524
Gene Symbol:
MTHFR
MTHFR
0.310
Biomarker
phenotype
CTD_human
Association study of four polymorphisms in three folate-related enzyme genes with non-obstructive male infertility.
16861746
2006
×
Entrez Id:
4548
Gene Symbol:
MTR
MTR
0.300
Biomarker
phenotype
CTD_human
Association study of four polymorphisms in three folate-related enzyme genes with non-obstructive male infertility.
16861746
2006
×
Entrez Id:
4552
Gene Symbol:
MTRR
MTRR
0.300
Biomarker
phenotype
CTD_human
Association study of four polymorphisms in three folate-related enzyme genes with non-obstructive male infertility.
16861746
2006
×
Entrez Id:
1811
Gene Symbol:
SLC26A3
SLC26A3
0.040
Biomarker
phenotype
BEFREE
Disruption of the SLC26A3 -mediated anion transport is associated with male subfertility .
16412765
2006
×
Entrez Id:
1811
Gene Symbol:
SLC26A3
SLC26A3
0.040
Biomarker
phenotype
BEFREE
A putative role of a primary anion exchange defect of SLC26A3 in male subfertility and the decline of renal function due to chronic dehydration deserve further characterization.
16641574
2006
×
Entrez Id:
1811
Gene Symbol:
SLC26A3
SLC26A3
0.040
Biomarker
phenotype
BEFREE
Tissue-specific co-expression with CFTR and NHE3 supports diverse functions of SLC26A3 and may have an impact on pathophysiology of male subfertility both in CLD and in cystic fibrosis (CF), as well as spermatoceles.
16421216
2006
×
Entrez Id:
6550
Gene Symbol:
SLC9A3
SLC9A3
0.010
AlteredExpression
phenotype
BEFREE
Tissue-specific co-expression with CFTR and NHE3 supports diverse functions of SLC26A3 and may have an impact on pathophysiology of male subfertility both in CLD and in cystic fibrosis (CF), as well as spermatoceles.
16421216
2006
×
Entrez Id:
1080
Gene Symbol:
CFTR
CFTR
0.310
Biomarker
phenotype
CTD_human
Novel CFTR missense mutations in Brazilian patients with congenital absence of vas deferens: counseling issues.
17823699
2007
×
Entrez Id:
79730
Gene Symbol:
NSUN7
NSUN7
0.300
Biomarker
phenotype
CTD_human
Sperm motility defects and infertility in male mice with a mutation in Nsun7, a member of the Sun domain-containing family of putative RNA methyltransferases.
17442852
2007
×
Entrez Id:
6795
Gene Symbol:
AURKC
AURKC
0.300
Biomarker
phenotype
CTD_human
Homozygous mutation of AURKC yields large-headed polyploid spermatozoa and causes male infertility.
17435757
2007
×
Entrez Id:
367
Gene Symbol:
AR
AR
0.320
Biomarker
phenotype
CTD_human
Genetic diagnosis in infertile men with numerical and constitutional sperm abnormalities.
18554162
2008
×
Entrez Id:
1080
Gene Symbol:
CFTR
CFTR
0.310
Biomarker
phenotype
CTD_human
Genetic diagnosis in infertile men with numerical and constitutional sperm abnormalities.
18554162
2008