scleroderma, systemic Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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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