Synovitis Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A connective tissue disease that results_in inflammation located_in synovial membrane that lines a synovial joint which causes pain and swelling. (Human Disease Ontology, DOID_2703)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D013585
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Genes

17 genes/proteins associated with the disease Synovitis from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
HLA-B major histocompatibility complex, class I, B 2.88009
COL2A1 collagen, type II, alpha 1 2.88009
POMC proopiomelanocortin 2.88009
IL1B interleukin 1, beta 1.43974
NOS2 nitric oxide synthase 2, inducible 1.24496
IL1A interleukin 1, alpha 1.21468
IL4 interleukin 4 1.18391
IL6 interleukin 6 1.16104
IL10 interleukin 10 1.1403
TGFB1 transforming growth factor, beta 1 1.09786
VCAM1 vascular cell adhesion molecule 1 1.08161
FAS Fas cell surface death receptor 1.06008
FAM19A5 family with sequence similarity 19 (chemokine (C-C motif)-like), member A5 1.04684
MPO myeloperoxidase 1.04611
SLIT1 slit homolog 1 (Drosophila) 1.03084
TNF tumor necrosis factor 1.02114
CCL2 chemokine (C-C motif) ligand 2 1.02077