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IFNGR2

This gene (IFNGR2) encodes the non-ligand-binding beta chain of the gamma interferon receptor. Human interferon-gamma receptor is a heterodimer of IFNGR1 and IFNGR2. Defects in IFNGR2 are a cause of mendelian susceptibility to mycobacterial disease (MSMD), also known as familial disseminated atypical mycobacterial infection. MSMD is a genetically heterogeneous disease with autosomal recessive, autosomal dominant or X-linked inheritance.
Protein class

Disease related genes, FDA approved drug targets, Human disease related genes

Predicted location

Membrane

Single cell type specificity

Cell type enhanced (Urothelial cells, Prostatic glandular cells)

Immune cell specificity

Immune cell enhanced (neutrophil)

Cell line specificity

Cell line enhanced (HDLM-2)

Interaction

Heterodimer with IFNGR1, to form the IFNG receptor complex (PubMed:7615558). Interacts (via intracellular domain) with JAK2 (PubMed:7615558, PubMed:7673114).

Molecular function

Receptor

More Types Infomation

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For Research Use Only. Not For Clinical Use.

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