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. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| IFNGR2-20-RE | 20 (40 μL) | 200 μL |  |
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| IFNGR2-20-OR | 20 (40 μL) | 200 μL |  |
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| IFNGR2-20-GO | 20 (40 μL) | 200 μL |  |
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| IFNGR2-20-GR | 20 (40 μL) | 200 μL |  |
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| IFNGR2-20-AQ | 20 (40 μL) | 200 μL |  |
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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. [provided by RefSeq, Jul 2008]
Gene Symbol : IFNGR2
Gene Name : Interferon gamma receptor 2
Chromosome : CHR 21: 334,028,95-334,375,20
Locus : 21q22.11
Alt. Genes : ABI2
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