Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 348751
Gene Symbol: FTCDNL1
FTCDNL1
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.120 GeneticVariation GWASDB Common variants in a novel gene, FONG on chromosome 2q33.1 confer risk of osteoporosis in Japanese. 21573128

2011

Entrez Id: 5906
Gene Symbol: RAP1A
RAP1A
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.110 GeneticVariation GWASDB An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits. 20548944

2010

Entrez Id: 501
Gene Symbol: ALDH7A1
ALDH7A1
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.110 GeneticVariation GWASDB Genome-wide association study identifies ALDH7A1 as a novel susceptibility gene for osteoporosis. 20072603

2010

Entrez Id: 654170
Gene Symbol: RPS16P8
RPS16P8
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.100 GeneticVariation GWASDB An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits. 20548944

2010

Entrez Id: 11138
Gene Symbol: TBC1D8
TBC1D8
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.100 GeneticVariation GWASDB An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits. 20548944

2010

Entrez Id: 2122
Gene Symbol: MECOM
MECOM
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.100 GeneticVariation GWASDB Meta-analysis identifies a MECOM gene as a novel predisposing factor of osteoporotic fracture. 23349225

2013

Entrez Id: 114876
Gene Symbol: OSBPL1A
OSBPL1A
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.100 GeneticVariation GWASDB An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits. 20548944

2010

Entrez Id: 643329
Gene Symbol: KRT18P57
KRT18P57
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.100 GeneticVariation GWASDB An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits. 20548944

2010

Entrez Id: 220164
Gene Symbol: DOK6
DOK6
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.100 GeneticVariation GWASDB An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits. 20548944

2010

Entrez Id: 4041
Gene Symbol: LRP5
LRP5
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.900 Biomarker GENOMICS_ENGLAND

Entrez Id: 1277
Gene Symbol: COL1A1
COL1A1
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.700 Biomarker GENOMICS_ENGLAND

Entrez Id: 1277
Gene Symbol: COL1A1
COL1A1
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.700 Biomarker GENOMICS_ENGLAND

Entrez Id: 1278
Gene Symbol: COL1A2
COL1A2
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.670 Biomarker GENOMICS_ENGLAND

Entrez Id: 8544
Gene Symbol: PIR
PIR
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.300 Biomarker GENOMICS_ENGLAND Sex-specific effect of Pirin gene on bone mineral density in a cohort of 4000 Chinese. 19766747

2010

Entrez Id: 10014
Gene Symbol: HDAC5
HDAC5
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.300 Biomarker GENOMICS_ENGLAND MicroRNA variants as genetic determinants of bone mass. 26723575

2016

Entrez Id: 7471
Gene Symbol: WNT1
WNT1
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.700 GeneticVariation UNIPROT In addition, in a family affected by dominantly inherited early-onset osteoporosis, a heterozygous WNT1 missense mutation was identified in affected individuals. 23499309

2013

Entrez Id: 7471
Gene Symbol: WNT1
WNT1
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.700 GeneticVariation UNIPROT In 10 family members with dominantly inherited, early-onset osteoporosis, we identified a heterozygous missense mutation in WNT1, c.652T→G (p.Cys218Gly). 23656646

2013

Entrez Id: 4041
Gene Symbol: LRP5
LRP5
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.900 Therapeutic RGD Zuogui Pill can prevent and treat glucocorticoid-induced osteoporosis in rats by up-regulating the expression of the key signal molecules Wnt1, LRP-5 and beta-catenin in Wnt signal transduction pathway. 21977807

2011

Entrez Id: 4041
Gene Symbol: LRP5
LRP5
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.900 Therapeutic RGD Effects of pulsed electromagnetic fields on bone mass and Wnt/β-catenin signaling pathway in ovariectomized rats. 22704852

2012

Entrez Id: 5741
Gene Symbol: PTH
PTH
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.600 Therapeutic RGD Role of phytoestrogenic oils in alleviating osteoporosis associated with ovariectomy in rats. 23161222

2013

Entrez Id: 7040
Gene Symbol: TGFB1
TGFB1
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.600 Therapeutic RGD Growth hormone treatment prevents osteoporosis in uremic rats. 17647196

2007

Entrez Id: 5741
Gene Symbol: PTH
PTH
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.600 Biomarker RGD The bone-protective effect of genistein in the animal model of bilateral ovariectomy: roles of phytoestrogens and PTH/PTHR1 against post-menopausal osteoporosis. 22312238

2012

Entrez Id: 2100
Gene Symbol: ESR2
ESR2
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.400 Therapeutic RGD [The expression of estrogen receptor alpha and beta in the intervention of different estrogens in rat bone metabolism]. 16955786

2006

Entrez Id: 3479
Gene Symbol: IGF1
IGF1
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.400 Biomarker RGD Diabetic bone disease. Low turnover osteoporosis related to decreased IGF-I production. 1466160

1992

Entrez Id: 3479
Gene Symbol: IGF1
IGF1
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.400 Biomarker RGD Etiopathogenesis of hepatic osteodystrophy in Wistar rats with cholestatic liver disease. 19424739

2009