Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6046
Gene Symbol: BRD2
BRD2
0.070 AlteredExpression disease BEFREE Chromatin-positive Klinefelter's syndrome with undetectable peripheral FSH levels. 1166860 1975
Entrez Id: 3730
Gene Symbol: ANOS1
ANOS1
0.010 Biomarker disease BEFREE The relation of patients with HHA to those with Klinefelter syndrome was 1:10 (n = 19/186). 3101500 1987
Entrez Id: 174
Gene Symbol: AFP
AFP
0.010 Biomarker disease BEFREE We recommend that all males with KS and early sexual development or with "normal" testicular growth be screened with measurement of germ cell tumor markers including beta-subunit of human chorionic gonadotropin and alpha-fetoprotein. 7535510 1995
Entrez Id: 7503
Gene Symbol: XIST
XIST
0.020 AlteredExpression disease BEFREE Thus, diagnosis of Klinefelter's syndrome can be accelerated without loss of sensitivity and specificity by detection of XIST expression in peripheral blood leukocytes. 8085664 1994
Entrez Id: 6046
Gene Symbol: BRD2
BRD2
0.070 AlteredExpression disease BEFREE Plasma LH and FSH levels were abnormally high and testosterone levels were reduced in all the patients with Klinefelter's syndrome. 10202890 1999
Entrez Id: 1617
Gene Symbol: DAZ1
DAZ1
0.010 GeneticVariation disease BEFREE Microdeletion of the DAZ (deleted in azoospermia) gene or the YRRM (Y chromosome ribonucleic acid recognition motif) gene does not occur in patients with Klinefelter's syndrome with and without spermatogenesis. 10202890 1999
Entrez Id: 5944
Gene Symbol: RBMY1HP
RBMY1HP
0.010 Biomarker disease BEFREE To evaluate the occurrence of microdeletions of the Y chromosome involving the DAZ and YRRM genes in patients with Klinefelter's syndrome with and without spermatogenesis. 10202890 1999
Entrez Id: 367
Gene Symbol: AR
AR
0.060 Biomarker disease BEFREE An AR gene abnormality does not constitute an important factor for impaired spermatogenesis in patients with Klinefelter's syndrome. 11473958 2001
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
0.020 GeneticVariation disease BEFREE Males who have MECP2 mutations and Klinefelter syndrome or who are mosaic for the mutation are more likely to present with a RTT-like phenotype. 11738861 2001
Entrez Id: 6462
Gene Symbol: SHBG
SHBG
0.010 Biomarker disease BEFREE ABP profiles were significantly smaller in men with Klinefelter's syndrome who were negative for spermatozoa compared with men who were positive. 11925377 2002
Entrez Id: 26
Gene Symbol: AOC1
AOC1
0.010 Biomarker disease BEFREE ABP profiles were significantly smaller in men with Klinefelter's syndrome who were negative for spermatozoa compared with men who were positive. 11925377 2002
Entrez Id: 4128
Gene Symbol: MAOA
MAOA
0.010 Biomarker disease BEFREE Since MAOA is X-linked, the heterozygotes are probable cases of Klinefelter's syndrome (47,XXY) suggesting that X-chromosome aneuploidy may increase the risk for developing type 2 alcoholism. 11927135 2002
Entrez Id: 2153
Gene Symbol: F5
F5
0.010 GeneticVariation disease BEFREE Severe venous thromboembolism in a young man with Klinefelter's syndrome and heterozygosis for both G20210A prothrombin and factor V Leiden mutations. 12544736 2003
Entrez Id: 2147
Gene Symbol: F2
F2
0.010 GeneticVariation disease BEFREE Severe venous thromboembolism in a young man with Klinefelter's syndrome and heterozygosis for both G20210A prothrombin and factor V Leiden mutations. 12544736 2003
Entrez Id: 6046
Gene Symbol: BRD2
BRD2
0.070 Biomarker disease BEFREE When non-KS oligo-azoospermic patients were classified according to histology [Sertoli cell-only (SCO), n = 18 or non-Sertoli cell only (non-SCO), n= 18] and compared to KS patients, the hormonal pattern did not differ between SCO and non-SCO subjects, but levels in KS patients were significantly different for FSH, inhibin-B and the FSH/inhibin-B ratio. 12864799 2003
Entrez Id: 6473
Gene Symbol: SHOX
SHOX
0.020 GeneticVariation disease BEFREE Tall stature, insulin resistance, and disturbed behavior in a girl with the triple X syndrome harboring three SHOX genes: offspring of a father with mosaic Klinefelter syndrome but with two maternal X chromosomes. 14752208 2004
Entrez Id: 268
Gene Symbol: AMH
AMH
0.030 AlteredExpression disease BEFREE Inhibin B and anti-Müllerian hormone, but not testosterone levels, are normal in infants with nonmosaic Klinefelter syndrome. 15070957 2004
Entrez Id: 354
Gene Symbol: KLK3
KLK3
0.020 GeneticVariation disease BEFREE In this article, we report a case of adenocarcinoma of the prostate in a 56-year-old man with Klinefelter syndrome (47,XXY) and non-Hodgkin lymphoma, as well as the AR and PSA genotype. 15350307 2004
Entrez Id: 29968
Gene Symbol: PSAT1
PSAT1
0.010 GeneticVariation disease BEFREE In this article, we report a case of adenocarcinoma of the prostate in a 56-year-old man with Klinefelter syndrome (47,XXY) and non-Hodgkin lymphoma, as well as the AR and PSA genotype. 15350307 2004
Entrez Id: 5324
Gene Symbol: PLAG1
PLAG1
0.010 GeneticVariation disease BEFREE In this article, we report a case of adenocarcinoma of the prostate in a 56-year-old man with Klinefelter syndrome (47,XXY) and non-Hodgkin lymphoma, as well as the AR and PSA genotype. 15350307 2004
Entrez Id: 5627
Gene Symbol: PROS1
PROS1
0.010 GeneticVariation disease BEFREE In this article, we report a case of adenocarcinoma of the prostate in a 56-year-old man with Klinefelter syndrome (47,XXY) and non-Hodgkin lymphoma, as well as the AR and PSA genotype. 15350307 2004
Entrez Id: 9520
Gene Symbol: NPEPPS
NPEPPS
0.010 GeneticVariation disease BEFREE In this article, we report a case of adenocarcinoma of the prostate in a 56-year-old man with Klinefelter syndrome (47,XXY) and non-Hodgkin lymphoma, as well as the AR and PSA genotype. 15350307 2004
Entrez Id: 2056
Gene Symbol: EPO
EPO
0.010 Biomarker disease BEFREE Erythropoietin-resistant anaemia in a predialysis patient with Klinefelter syndrome. 15877674 2005
Entrez Id: 4204
Gene Symbol: MECP2
MECP2
0.020 GeneticVariation disease BEFREE However, mutations in MECP2 also have been identified in normal carrier female individuals, female individuals with mild learning disabilities and features of Angelman syndrome, and male individuals with Klinefelter syndrome or Rett syndrome-like features, fatal neonatal encephalopathy, and familial X-linked mental retardation with or without motor abnormalities. 16225824 2005
Entrez Id: 25797
Gene Symbol: QPCT
QPCT
0.010 Biomarker disease BEFREE We present clinical data on a boy with KS and sexual precocity, and summarize the published data on 12 boys with KS out of 54 cases of KS and M-GCT. 16470792 2006