cd3epsilon deficiency Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A severe combined immunodeficiency that is an autosomal recessive immunodeficiency caused by mutations in the gene coding for T-cell surface glycoprotein CD3epsilon chain precursors. Patients with CD3epsilon deficiency have a severe defect in the expression of the T-cell receptor CD3-complex. (Human Disease Ontology, DOID_0060017)
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6 genes co-occuring with the disease cd3epsilon deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
CD3D CD3d molecule, delta (CD3-TCR complex) 1.75505
CD3G CD3g molecule, gamma (CD3-TCR complex) 1.5238
CD3E CD3e molecule, epsilon (CD3-TCR complex) 1.37817
TAL1 T-cell acute lymphocytic leukemia 1 1.12066
LMO1 LIM domain only 1 (rhombotin 1) 0.821257
CDKN2A cyclin-dependent kinase inhibitor 2A 0.362239