Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3293
Gene Symbol: HSD17B3
HSD17B3
0.410 Biomarker disease CTD_human 17beta-hydroxysteroid dehydrogenase-3 deficiency: a rare endocrine cause of male-to-female sex reversal. 17071532 2006
Entrez Id: 3293
Gene Symbol: HSD17B3
HSD17B3
0.410 GeneticVariation disease BEFREE A (R80Q) mutation in 17 beta-hydroxysteroid dehydrogenase type 3 gene among Arabs of Israel is associated with pseudohermaphroditism in males and normal asymptomatic females. 8626842 1996
Entrez Id: 3293
Gene Symbol: HSD17B3
HSD17B3
0.410 GeneticVariation disease CLINVAR
Entrez Id: 3293
Gene Symbol: HSD17B3
HSD17B3
0.410 CausalMutation disease CLINVAR
Entrez Id: 3973
Gene Symbol: LHCGR
LHCGR
0.400 Biomarker disease CTD_human Proposed role for COUP-TFII in regulating fetal Leydig cell steroidogenesis, perturbation of which leads to masculinization disorders in rodents. 22615892 2012
Entrez Id: 3973
Gene Symbol: LHCGR
LHCGR
0.400 CausalMutation disease CLINVAR
Entrez Id: 1646
Gene Symbol: AKR1C2
AKR1C2
0.300 Biomarker disease CTD_human The aldo-keto reductases (AKRs): Overview. 25304492 2015
Entrez Id: 8644
Gene Symbol: AKR1C3
AKR1C3
0.300 Biomarker disease CTD_human The aldo-keto reductases (AKRs): Overview. 25304492 2015
Entrez Id: 1645
Gene Symbol: AKR1C1
AKR1C1
0.300 Biomarker disease CTD_human The aldo-keto reductases (AKRs): Overview. 25304492 2015
Entrez Id: 11036
Gene Symbol: GTF2A1L
GTF2A1L
0.100 CausalMutation disease CLINVAR
Entrez Id: 105376162
Gene Symbol: HSD17B3-AS1
HSD17B3-AS1
0.100 CausalMutation disease CLINVAR
Entrez Id: 286749
Gene Symbol: STON1-GTF2A1L
STON1-GTF2A1L
0.100 CausalMutation disease CLINVAR
Entrez Id: 6716
Gene Symbol: SRD5A2
SRD5A2
0.020 GeneticVariation disease BEFREE We found an SRD5A2 gene mutation in exon 5, where arginine is substituted with glutamine (R246Q), in two males with pseudohermaphroditism and ambiguous genitalia from unrelated families. 18097518 2008
Entrez Id: 6716
Gene Symbol: SRD5A2
SRD5A2
0.020 GeneticVariation disease BEFREE A classification based on the severity of the masculinization defect may be used for correlation of phenotypes with enzyme activities and genotypes, and for comparisons of phenotypes between different patients as the basis for clinical decisions to be made in patients with pseudohermaphroditism due to steroid 5 alpha-reductase 2 deficiency. 8723114 1996
Entrez Id: 7166
Gene Symbol: TPH1
TPH1
0.010 Biomarker disease BEFREE Of the three species with data on the relative timing of gonad differentiation and genital dimorphism, the females of two (Niveoscincus ocellatus and Barisia imbricata) exhibit a phase of temporary pseudohermaphroditism or TPH (gonads have differentiated well before genital dimorphism). 30291276 2018
Entrez Id: 284654
Gene Symbol: RSPO1
RSPO1
0.010 Biomarker disease BEFREE To elucidate the role of Rspo1 as a candidate female-determining gene in a mouse model, we generated Rspo1-null (Rspo1(-/-)) mice and found that Rspo1(-/-) XX mice displayed masculinized features including pseudohermaphroditism in genital ducts, depletion of fetal oocytes, male-specific coelomic vessel formation and ectopic testosterone production in the ovaries. 18250097 2008
Entrez Id: 1586
Gene Symbol: CYP17A1
CYP17A1
0.010 GeneticVariation disease BEFREE P450c17 deficiency (17OHD), caused by mutation in CYP17A1 gene, is characterized by severe hypertension-hypokalemia, sexual infantilism in females, and pseudohermaphroditism in males. 16772352 2006
Entrez Id: 7490
Gene Symbol: WT1
WT1
0.010 GeneticVariation disease BEFREE Denys-Drash syndrome (DDS) is associated with mutations of the Wilms' tumour 1 (WT1) gene, and is characterized by pseudohermaphroditism, a progressive glomerulopathy, and the development of Wilms' tumour. 14671061 2004
Entrez Id: 268
Gene Symbol: AMH
AMH
0.010 GeneticVariation disease BEFREE Mutations in mullerian inhibiting substance (MIS) or MISRII cause male sexual abnormalities, persistent mullerian duct syndrome, and pseudohermaphroditism. 12724325 2003
Entrez Id: 269
Gene Symbol: AMHR2
AMHR2
0.010 GeneticVariation disease BEFREE Mutations in mullerian inhibiting substance (MIS) or MISRII cause male sexual abnormalities, persistent mullerian duct syndrome, and pseudohermaphroditism. 12724325 2003
Entrez Id: 1588
Gene Symbol: CYP19A1
CYP19A1
0.010 GeneticVariation disease BEFREE Here we report a novel homozygous aromatase mutation (Val370-to-Met) found in a girl with pseudohermaphroditism (Prader V). 9829218 1999