Entity Details

Primary name INGR1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionP15260
EntryNameINGR1_HUMAN
FullNameInterferon gamma receptor 1
TaxID9606
Evidenceevidence at protein level
Length489
SequenceStatuscomplete
DateCreated1990-04-01
DateModified2021-06-02

Ontological Relatives

GenesIFNGR1

GO terms

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GOName
GO:0001774 microglial cell activation
GO:0004896 cytokine receptor activity
GO:0004906 interferon-gamma receptor activity
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0007165 signal transduction
GO:0009615 response to virus
GO:0010628 positive regulation of gene expression
GO:0016021 integral component of membrane
GO:0019221 cytokine-mediated signaling pathway
GO:0019955 cytokine binding
GO:0032760 positive regulation of tumor necrosis factor production
GO:0048143 astrocyte activation
GO:0060333 interferon-gamma-mediated signaling pathway
GO:0060334 regulation of interferon-gamma-mediated signaling pathway
GO:1900222 negative regulation of amyloid-beta clearance
GO:1902004 positive regulation of amyloid-beta formation

Subcellular Location

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Subcellular Location
Cell membrane

Domains

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DomainNameCategoryType
IPR003961 Fibronectin type IIIDomainDomain
IPR008355 Interferon gamma receptor alpha subunitFamilyFamily
IPR013783 Immunoglobulin-like foldFamilyHomologous superfamily
IPR021126 Interferon gamma receptor, poxvirus/mammalDomainDomain
IPR036116 Fibronectin type III superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
209950 OMIMImmunodeficiency 27A (IMD27A)A form of Mendelian susceptibility to mycobacterial disease, a rare condition caused by impairment of interferon-gamma mediated immunity. It is characterized by predisposition to illness caused by moderately virulent mycobacterial species, such as Bacillus Calmette-Guerin (BCG) vaccine, environmental non-tuberculous mycobacteria, and by the more virulent Mycobacterium tuberculosis. Other microorganisms rarely cause severe clinical disease in individuals with susceptibility to mycobacterial infections, with the exception of Salmonella which infects less than 50% of these individuals. Clinical outcome severity depends on the degree of impairment of interferon-gamma mediated immunity. Some patients die of overwhelming mycobacterial disease with lepromatous-like lesions in early childhood, whereas others develop, later in life, disseminated but curable infections with tuberculoid granulomas. The disease is caused by variants affecting the gene represented in this entry.
615978 OMIMImmunodeficiency 27B (IMD27B)A form of Mendelian susceptibility to mycobacterial disease, a rare condition caused by impairment of interferon-gamma mediated immunity. It is characterized by predisposition to illness caused by moderately virulent mycobacterial species, such as Bacillus Calmette-Guerin (BCG) vaccine, environmental non-tuberculous mycobacteria, and by the more virulent Mycobacterium tuberculosis. Other microorganisms rarely cause severe clinical disease in individuals with susceptibility to mycobacterial infections, with the exception of Salmonella which infects less than 50% of these individuals. Clinical outcome severity depends on the degree of impairment of interferon-gamma mediated immunity. Some patients die of overwhelming mycobacterial disease with lepromatous-like lesions in early childhood, whereas others develop, later in life, disseminated but curable infections with tuberculoid granulomas. IMD27B commonly presents with recurrent, moderately severe infections with environmental mycobacteria or BCG. Salmonellosis is present in about 5% of patients. The disease is caused by variants affecting the gene represented in this entry.

Drugs

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DrugNameSourceType
DB00033 Interferon gamma-1bDrugbankbiotech