Entity Details

Primary name ICOS
Entity type gene
Source Source Link

Details

PrimaryID29851
RefseqGeneNG_011586
SymbolICOS
Nameinducible T cell costimulator
Chromosome2
Location2q33.2
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2000-02-21
ModificationDate2021-06-13

Ontological Relatives

UniProt IDsICOS_HUMAN

GO terms

Show/Hide Table
GOName
GO:0002517 T cell tolerance induction
GO:0005576 extracellular region
GO:0005886 plasma membrane
GO:0006955 immune response
GO:0016021 integral component of membrane
GO:0031295 T cell costimulation
GO:0051897 positive regulation of protein kinase B signaling
GO:0098609 cell-cell adhesion

Diseases

Show/Hide Table
Disease IDSourceNameDescription
607594 OMIMImmunodeficiency, common variable, 1 (CVID1)A primary immunodeficiency characterized by antibody deficiency, hypogammaglobulinemia, recurrent bacterial infections and an inability to mount an antibody response to antigen. The defect results from a failure of B-cell differentiation and impaired secretion of immunoglobulins; the numbers of circulating B-cells is usually in the normal range, but can be low. The disease is caused by variants affecting the gene represented in this entry.