1. Gene
  2. ICOS - inducible T cell costimulator Gene

ICOS - inducible T cell costimulator Gene

Homo sapiens

Also known as AILIM; CD278; CVID1

Gene ID: 29851 | Gene type: protein coding

About ICOS

Cytogenetic location: 2q33.2 Genomic coordinates (GRCh38): 2:203,936,763-203,961,577 (from NCBI)

This gene has 2 transcripts (splice variants), 115 orthologues and is associated with 3 phenotypes. Biased expression in lymph node (RPKM 7.8), bone marrow (RPKM 6.5) and 9 other tissues.

Summary

The protein encoded by this gene belongs to the CD28 and CTLA-4 cell-surface receptor family. It forms homodimers and plays an important role in cell-cell signaling, immune responses, and regulation of cell proliferation. [provided by RefSeq, Jul 2008]

ICOS Products(1)

mRNA Protein Name
NM_012092.4 NP_036224.1 inducible T-cell costimulator precursor
Protein Preferred Names Protein Names

inducible T-cell costimulator

activation-inducible lymphocyte immunomediatory molecule

Recombinant ICOS Proteins

Cat. No. Product Name Accession Purity
HY-P72618 ICOS Protein, Human (121a.a, HEK293, Fc) Q9Y6W8-1 (E21-F141) ≥95%
HY-P76396 ICOS Protein, Human (HEK293, His-Fc) Q9Y6W8-1 (E21-F141) ≥95%
HY-P78546 ICOS Protein, Human (C136S, C137S, HEK293, His) Q9Y6W8-1 (E21-F141, C136S, C137S) ≥95%

Related Diseases

Diseases Alias
Immunodeficiency, Common Variable, 1

CVID1

Antibody Deficiency Due To Icos Defect

Icos Deficiency

Common Variable Immunodeficiency 1

Immunodeficiency, Variable, Common, Type 1

Common Variable Immunodeficiency

Cvid

Common Variable Agammaglobulinemia

Common Variable Immune Deficiency

Acquired Hypogammaglobulinemia

Hypogamma-Globulinemia, Acquired

Idiopathic Immunoglobulin Deficiency

Primary Antibody Deficiency

Primary Hypogammaglobulinemia

Acquired Agammaglobulinemia

Sporadic Hypogammaglobulinemia

Common Variable Hypogamma-Globulinemia

Immunoglobulin Deficiency, Late-Onset

Common Variable Hypogammaglobulinemia

Immunodeficiency, Common Variable

Immunodeficiency, Common Variable, 2

CVID2

Antibody Deficiency Due To Taci Defect

Hypogammaglobulinemia Due To Taci Deficiency

Common Variable Immunodeficiency 2

Immunodeficiency, Variable, Common, Type 2

Dermatitis, Atopic, 5

ATOD5

Atopic Dermatitis 5

Dermatitis, Atopic, Susceptibility To, 5

Dermatitis, Atopic 5

Systemic Lupus Erythematosus

Lupus Nephritis

SLE

Disseminated Lupus Erythematosus

Systemic Lupus Erythematosus, Susceptibility To

Lupus Erythematosus, Systemic

Lupus Nephritis, Susceptibility To

Libman-Sacks Disease

Systemic Lupus Erythematosus Susceptibility To

Sle - Lupus Erythematosus, Systemic

Le Syndrome

Lupus

Lupus Erythematosus Systemic

Lupus Erythematosus, Systemic, Susceptibility To

Lupus Vulgaris

Lupus Erythematosus, Discoid

Lupus Erythematosus

Systemic Lupus Erythematosus Nos

Sle - [Systemic Lupus Erythematosus]

Inflammatory Bowel Disease

Inflammatory Bowel Diseases

Bowel Disease, Inflammatory

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus ICOS RGD RGD:620123
Canis familiaris ICOS VGNC VGNC:41861
Mus musculus ICOS MGD MGI:1858745
Macaca mulatta ICOS VGNC VGNC:73555
Bos taurus ICOS VGNC VGNC:30030
Felis catus ICOS VGNC VGNC:80240
Macaca fascicularis ICOS NCBI NCBI:102116512
Others ICOS NCBI