×
Entrez Id:
1589
Gene Symbol:
CYP21A2
CYP21A2
0.100
GeneticVariation
disease
GWASDB
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus.
20383147
2010
HLA-DQB2
0.100
GeneticVariation
disease
GWASDB
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus.
20383147
2010
HLA-DPA2
0.100
GeneticVariation
disease
GWASDB
HLA-DPB1 and DPB2 are genetic loci for systemic sclerosis: a genome-wide association study in Koreans with replication in North Americans.
19950302
2009
×
Entrez Id:
84872
Gene Symbol:
ZC3H10
ZC3H10
0.100
GeneticVariation
disease
GWASDB
Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.
21779181
2011
×
Entrez Id:
23344
Gene Symbol:
ESYT1
ESYT1
0.100
GeneticVariation
disease
GWASDB
Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.
21779181
2011
MSH5-SAPCD1
0.100
GeneticVariation
disease
GWASDB
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus.
20383147
2010
×
Entrez Id:
57661
Gene Symbol:
PHRF1
PHRF1
0.100
GeneticVariation
disease
GWASDB
A systemic sclerosis and systemic lupus erythematosus pan-meta-GWAS reveals new shared susceptibility loci.
23740937
2013
LINC01500
0.100
GeneticVariation
disease
GWASDB
A systemic sclerosis and systemic lupus erythematosus pan-meta-GWAS reveals new shared susceptibility loci.
23740937
2013
×
Entrez Id:
177
Gene Symbol:
AGER
AGER
0.100
GeneticVariation
disease
GWASDB
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus.
20383147
2010
HLA-DPA1
0.100
GeneticVariation
disease
GWASDB
Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.
21779181
2011
×
Entrez Id:
4439
Gene Symbol:
MSH5
MSH5
0.100
GeneticVariation
disease
GWASDB
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus.
20383147
2010
×
Entrez Id:
8859
Gene Symbol:
STK19
STK19
0.100
GeneticVariation
disease
GWASDB
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus.
20383147
2010
×
Entrez Id:
23294
Gene Symbol:
ANKS1A
ANKS1A
0.100
GeneticVariation
disease
GWASDB
A systemic sclerosis and systemic lupus erythematosus pan-meta-GWAS reveals new shared susceptibility loci.
23740937
2013
×
Entrez Id:
219285
Gene Symbol:
SAMD9L
SAMD9L
0.100
GeneticVariation
disease
GWASDB
A systemic sclerosis and systemic lupus erythematosus pan-meta-GWAS reveals new shared susceptibility loci.
23740937
2013
×
Entrez Id:
100507679
Gene Symbol:
MUC22
MUC22
0.100
GeneticVariation
disease
GWASDB
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus.
20383147
2010
×
Entrez Id:
1133
Gene Symbol:
CHRM5
CHRM5
0.100
GeneticVariation
disease
GWASDB
A systemic sclerosis and systemic lupus erythematosus pan-meta-GWAS reveals new shared susceptibility loci.
23740937
2013
PSORS1C2
0.100
GeneticVariation
disease
GWASDB
Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis.
21750679
2011
LINC01924
0.100
GeneticVariation
disease
GWASDB
A systemic sclerosis and systemic lupus erythematosus pan-meta-GWAS reveals new shared susceptibility loci.
23740937
2013
LINC00305
0.100
GeneticVariation
disease
GWASDB
A systemic sclerosis and systemic lupus erythematosus pan-meta-GWAS reveals new shared susceptibility loci.
23740937
2013
×
Entrez Id:
3122
Gene Symbol:
HLA-DRA
HLA-DRA
0.100
GeneticVariation
disease
GWASDB
Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.
21779181
2011
×
Entrez Id:
3305
Gene Symbol:
HSPA1L
HSPA1L
0.100
GeneticVariation
disease
GWASDB
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus.
20383147
2010
×
Entrez Id:
2887
Gene Symbol:
GRB10
GRB10
0.100
GeneticVariation
disease
GWASDB
Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.
21779181
2011
×
Entrez Id:
64132
Gene Symbol:
XYLT2
XYLT2
0.300
Biomarker
disease
GENOMICS_ENGLAND
×
Entrez Id:
51317
Gene Symbol:
PHF21A
PHF21A
0.300
Biomarker
disease
GENOMICS_ENGLAND
De novo truncating variants in PHF21A cause intellectual disability and craniofacial anomalies.
30487643
2019
×
Entrez Id:
1435
Gene Symbol:
CSF1
CSF1
0.230
Biomarker
disease
RGD
This study shows that the increased number of macrophages with heterogeneous immunophenotypes, which might be induced by MCP-1 and CSF-1 , could participate in the sclerotic lesion formation, presumably through increased fibrogenic factors such as galectin-3 and TGF-β1; the data may provide useful information to understand the pathogenesis of the human scleroderma condition.
22700848
2013