scleroderma, systemic Gene Set
Dataset
GAD Gene-Disease Associations
Category
disease or phenotype associations
Type
disease
Similar Terms
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Genes
29 genes associated with the disease scleroderma, systemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Symbol
Name
BANK1
B-cell scaffold protein with ankyrin repeats 1
CCL2
chemokine (C-C motif) ligand 2
CD247
CD247 molecule
COL15A1
collagen, type XV, alpha 1
CTGF
connective tissue growth factor
ESR1
estrogen receptor 1
ESR2
estrogen receptor 2 (ER beta)
FAS
Fas cell surface death receptor
FBN1
fibrillin 1
GRB10
growth factor receptor-bound protein 10
HLA-DPA1
major histocompatibility complex, class II, DP alpha 1
HLA-DPB1
major histocompatibility complex, class II, DP beta 1
HLA-DQA1
major histocompatibility complex, class II, DQ alpha 1
HLA-DQB1
major histocompatibility complex, class II, DQ beta 1
HLA-DRA
major histocompatibility complex, class II, DR alpha
HLA-DRB1
major histocompatibility complex, class II, DR beta 1
HTR2A
5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled
IFNG
interferon, gamma
IL10
interleukin 10
IL1R1
interleukin 1 receptor, type I
IL2
interleukin 2
IL23R
interleukin 23 receptor
IL6
interleukin 6
IRF5
interferon regulatory factor 5
NOTCH4
notch 4
PTPN22
protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
SOX5
SRY (sex determining region Y)-box 5
STAT4
signal transducer and activator of transcription 4
TNPO3
transportin 3