Sjogren's Syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A hypersensitivity reaction type II disease that involves attack of immune cells which destroy the exocrine glands that produce tears and saliva. (Human Disease Ontology, DOID_12894)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D012859
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Genes

12 genes/proteins associated with the disease Sjogren's Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
IRAK1BP1 interleukin-1 receptor-associated kinase 1 binding protein 1 2.88009
PHIP pleckstrin homology domain interacting protein 2.88009
GTF2I general transcription factor IIi 2.88009
FCGR2A Fc fragment of IgG, low affinity IIa, receptor (CD32) 2.88009
PTTG1 pituitary tumor-transforming 1 2.88009
TNIP1 TNFAIP3 interacting protein 1 2.88009
TNFAIP3 tumor necrosis factor, alpha-induced protein 3 2.88009
PRDM1 PR domain containing 1, with ZNF domain 2.88009
DGKQ diacylglycerol kinase, theta 110kDa 2.88009
IL12A interleukin 12A 2.88009
ITSN2 intersectin 2 2.88009
STAT4 signal transducer and activator of transcription 4 2.88009