Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 GeneticVariation group BEFREE More recently, however, it has emerged that heterozygous loss of function mutations in NR5A1 can be found relatively frequently in children and adults with 46,XY disorders of sex development (DSD) but with apparently normal adrenal function. 18987494 2008
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 GeneticVariation group BEFREE We have analyzed the gene encoding SF1 (NR5A1) in a cohort of 27 patients with 46,XY disorders of sex development (DSD) from the German network of DSD. 17694559 2008
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 GeneticVariation group BEFREE Mutational analysis of NR5A1 in 60 individuals with varying degrees of hypospadias from the German DSD network. 19439508 2009
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 GeneticVariation group BEFREE A novel heterozygous mutation of steroidogenic factor-1 (SF-1/Ad4BP) gene (NR5A1) in a 46, XY disorders of sex development (DSD) patient without adrenal failure. 19318730 2009
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 Biomarker group BEFREE Investigations of humans with disorders of sex development (DSDs) resulted in the discovery of many of the now-known mammalian sex-determining genes, including SRY, RSPO1, SOX9, NR5A1, WT1, NR0B1, and WNT4. 21129722 2010
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 GeneticVariation group BEFREE Mutation analysis of NR5A1 encoding steroidogenic factor 1 in 77 patients with 46, XY disorders of sex development (DSD) including hypospadias. 22028768 2011
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 GeneticVariation group BEFREE In human embryogenesis, loss of SRY (sex determining region on Y), SOX9 (SRY-related HMG box 9) or SF1 (steroidogenic factor 1) function causes disorders of sex development (DSD). 21412441 2011
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 Biomarker group BEFREE Multifunctional role of steroidogenic factor 1 and disorders of sex development. 22218443 2011
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 GeneticVariation group BEFREE As NR5A1 mutations can cause a wide spectrum of DSD with relatively high frequency, the analysis of the NR5A1 gene by MLPA is quite important and should be extended to larger groups of patients. 21654157 2011
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 GeneticVariation group BEFREE Karyotyping was done and the patients were screened for underlying changes in SRY, desert hedgehog (DHH), DAX1 (NR0B1) and SF1 (NR5A1) genes, mutations in which are implicated in DSD. 21242195 2011
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 GeneticVariation group BEFREE Testosterone production during puberty in two 46,XY patients with disorders of sex development and novel NR5A1 (SF-1) mutations. 22474171 2012
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 GeneticVariation group BEFREE NR5A1 mutations have been detected in 46,XY individuals with disorders of sexual development (DSD) but apparently normal adrenal function and in 46,XX women with normal sexual development yet primary ovarian insufficiency (POI). 22549935 2012
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 GeneticVariation group BEFREE Individuals with NR5A1 mutations encoding steroidogenic factor-1 (SF1) develop a phenotypically broad range of disorders of sexual development (DSD). 23969951 2013
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 Biomarker group BEFREE To date microdeletions involving NR5A1 have been reported in only two patients with DSDs. 24056159 2013
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 GeneticVariation group BEFREE Mutations identified by NR5A1 sequencing have been associated with disorders of sex development (DSD), ranging from sex reversal to severe hypospadias in 46,XY patients and premature ovarian failure (POF) in 46,XX patients. 23918653 2013
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 GeneticVariation group BEFREE NR5A1 loss-of-function mutations are increasingly found to be the cause of 46,XY disorders of sex development (DSD). 22909003 2013
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 GeneticVariation group BEFREE We investigate the frequency of NR5A1 mutations in an Egyptian cohort of XY DSD. 24591553 2014
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 GeneticVariation group BEFREE Both homozygous, compound heterozygous and heterozygous mutations in the NR5A1 gene may determine 46,XY disorders of sex development (DSD). 24434652 2014
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 GeneticVariation group BEFREE The identification of heterozygous individuals with this novel mutation may bring additional knowledge on structural modifications that may influence NR5A1 DNA-binding ability, and may also contribute to genotype-phenotype correlations in DSD. 24405868 2014
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 GeneticVariation group BEFREE Heterozygous mutations of NR5A1, which encodes steroidogenic factor 1 (SF1), were identified in patients with 46,XY disorders of sex development (DSD) with normal adrenal function. 26139438 2015
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 Biomarker group BEFREE In 46,XY individuals, NR5A1-related phenotypes may range from disorders of sex development (DSD) to oligo/azoospermia, and in 46,XX individuals, from 46,XX ovotesticular and testicular DSD to primary ovarian insufficiency (POI). 28033660 2016
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 GeneticVariation group BEFREE Mutations in human NR5A1 are frequently associated with 46,XY disorders of sex development (DSD). 26260161 2016
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 GeneticVariation group BEFREE Heterozygous SF1 loss-of-function mutations in these cases resulted in mild DSD manifestations, such as dysgenetic testes, spontaneous puberty, and preserved adrenal function. 27463801 2016
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 GeneticVariation group BEFREE A variant in steroidogenic factor-1 (SF-1, encoded by the gene NR5A1), p.Arg92Trp, has recently been reported in multiple families with 46,XX ovotesticular or testicular disorders of sex development (DSD). 27855412 2017
Entrez Id: 2516
Gene Symbol: NR5A1
NR5A1
0.100 GeneticVariation group BEFREE Mutations in NR5A1 have been reported as a frequent cause of 46,XY disorders of sex development (DSD) associated to a broad phenotypic spectrum ranging from infertility, ambiguous genitalia, anorchia to gonadal dygenesis and female genitalia. 28459839 2017