systemic scleroderma Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A scleroderma that is characterized by fibrosis (or hardening) of the skin and major organs, as well as vascular alterations, and autoantibodies. (Human Disease Ontology, DOID_418)
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Genes

6 genes involed in the disease systemic scleroderma from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
BANK1 B-cell scaffold protein with ankyrin repeats 1
BLK BLK proto-oncogene, Src family tyrosine kinase
IRF5 interferon regulatory factor 5
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
STAT4 signal transducer and activator of transcription 4
TNFSF4 tumor necrosis factor (ligand) superfamily, member 4