Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2798
Gene Symbol: GNRHR
GNRHR
1.000 Biomarker disease CTD_human
Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
0.500 GeneticVariation disease CLINVAR
Entrez Id: 6870
Gene Symbol: TACR3
TACR3
0.440 GeneticVariation disease CLINVAR
Entrez Id: 6866
Gene Symbol: TAC3
TAC3
0.440 GeneticVariation disease CLINVAR
Entrez Id: 55703
Gene Symbol: POLR3B
POLR3B
0.400 Biomarker disease CTD_human
Entrez Id: 55703
Gene Symbol: POLR3B
POLR3B
0.400 CausalMutation disease CLINVAR
Entrez Id: 55703
Gene Symbol: POLR3B
POLR3B
0.400 GeneticVariation disease CLINVAR
Entrez Id: 55717
Gene Symbol: WDR11
WDR11
0.340 Biomarker disease CTD_human
Entrez Id: 8822
Gene Symbol: FGF17
FGF17
0.310 Biomarker disease CTD_human
Entrez Id: 558
Gene Symbol: AXL
AXL
0.310 Biomarker disease CTD_human
Entrez Id: 10011
Gene Symbol: SRA1
SRA1
0.310 Biomarker disease CTD_human
Entrez Id: 285025
Gene Symbol: CCDC141
CCDC141
0.310 Biomarker disease CTD_human
Entrez Id: 9723
Gene Symbol: SEMA3E
SEMA3E
0.300 Biomarker disease CTD_human
Entrez Id: 389549
Gene Symbol: FEZF1
FEZF1
0.300 Biomarker disease CTD_human
Entrez Id: 23767
Gene Symbol: FLRT3
FLRT3
0.300 Biomarker disease CTD_human
Entrez Id: 54756
Gene Symbol: IL17RD
IL17RD
0.300 Biomarker disease CTD_human
Entrez Id: 1848
Gene Symbol: DUSP6
DUSP6
0.300 Biomarker disease CTD_human
Entrez Id: 81848
Gene Symbol: SPRY4
SPRY4
0.300 Biomarker disease CTD_human
Entrez Id: 3730
Gene Symbol: ANOS1
ANOS1
0.200 GeneticVariation disease CLINVAR
Entrez Id: 128674
Gene Symbol: PROKR2
PROKR2
0.160 GeneticVariation disease CLINVAR
Entrez Id: 9394
Gene Symbol: HS6ST1
HS6ST1
0.110 GeneticVariation disease CLINVAR
Entrez Id: 27241
Gene Symbol: BBS9
BBS9
0.100 CausalMutation disease CLINVAR
Entrez Id: 54476
Gene Symbol: RNF216
RNF216
0.100 GeneticVariation disease CLINVAR
Entrez Id: 10908
Gene Symbol: PNPLA6
PNPLA6
0.100 GeneticVariation disease CLINVAR
Entrez Id: 2796
Gene Symbol: GNRH1
GNRH1
0.380 GeneticVariation disease BEFREE We conclude that a major rearrangement of the GnRH gene is not a common basis for IHH in humans. 2546961 1989