1. Gene
  2. IFNGR2 - interferon gamma receptor 2 Gene

IFNGR2 - interferon gamma receptor 2 Gene

Homo sapiens

Also known as AF-1; IFGR2; IMD28; IFNGT1

Gene ID: 3460 | Gene type: protein coding

About IFNGR2

Cytogenetic location: 21q22.11 Genomic coordinates (GRCh38): 21:33,402,882-33,437,516 (from NCBI)

This gene has 7 transcripts (splice variants), 1 gene allele, 133 orthologues, 11 paralogues and is associated with 4 phenotypes. Ubiquitous expression in placenta (RPKM 30.0), appendix (RPKM 25.4) and 25 other tissues.

Summary

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]

IFNGR2 Products(2)

mRNA Protein Name
NM_001329128.2 NP_001316057.1 interferon gamma receptor 2 isoform 1 precursor
NM_005534.4 NP_005525.2 interferon gamma receptor 2 isoform 2 precursor
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
enables type II interferon receptor activity IDA
IDA: Inferred from direct assay
20015550 GOA
Biological Process GO Annotation Evidence Reference Source
involved in type III interferon-mediated signaling pathway IDA
IDA: Inferred from direct assay
20015550 GOA
Cellular Component GO Annotation Evidence Reference Source
is active in plasma membrane IDA
IDA: Inferred from direct assay
20015550 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

IFNGR2 Protein Structure

Tissue_fac

Tissue_fac: Tissue factor (10 - 126)

Interfer-bind

Interfer-bind: Interferon-alpha/beta receptor, fibronectin type III (140 - 237)

  • 0
  • 100
  • 200
  • 300
  • 337 a.a.
Protein Preferred Names Protein Names

interferon gamma receptor 2

IFN-gamma receptor 2

IFNGR2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
IFNGR2 P38484 RTP2 Homo sapiens Q5QGT7 32296183
Intra
IFNGR2 P38484 ZDHHC24 Homo sapiens Q6UX98 32296183
Intra
IFNGR2 P38484 TMEM199 Homo sapiens Q8N511 32296183
Intra
IFNGR2 P38484 JAGN1 Homo sapiens Q8N5M9 32296183
Intra
IFNGR2 P38484 ADIPOQ Homo sapiens Q15848 32296183
Intra
IFNGR2 P38484 ADIPOQ Homo sapiens Q15848 32296183
Intra
IFNGR2 P38484 ERMP1 Homo sapiens Q7Z2K6 32296183
Intra
IFNGR2 P38484 TMEM254 Homo sapiens Q8TBM7 32296183
Intra
IFNGR2 P38484 CLEC7A Homo sapiens Q9BXN2-6 32296183
Intra
IFNGR2 P38484 TMEM97 Homo sapiens Q5BJF2 32296183
Intra
IFNGR2 P38484 BRICD5 Homo sapiens Q6PL45-2 32296183
Intra
IFNGR2 P38484 CLDN19 Homo sapiens Q8N6F1-2 32296183
Intra
IFNGR2 P38484 SLC52A1 Homo sapiens Q9NWF4 32296183
Intra
IFNGR2 P38484 CD302 Homo sapiens Q8IX05 32296183
Intra
IFNGR2 P38484 TREX1 Homo sapiens Q9NSU2-1 32296183
Intra
IFNGR2 P38484 BTNL8 Homo sapiens Q6UX41-6 32296183
Intra
IFNGR2 P38484 TMEM140 Homo sapiens Q9NV12 32296183
Intra
IFNGR2 P38484 PMP22 Homo sapiens Q01453 32296183
Intra
IFNGR2 P38484 TMEM60 Homo sapiens Q9H2L4 32296183
Intra
IFNGR2 P38484 EMP3 Homo sapiens P54852 32296183
Intra
IFNGR2 P38484 CXCL9 Homo sapiens Q07325 32296183
Intra
IFNGR2 P38484 GIMAP5 Homo sapiens Q96F15 32296183
Intra
IFNGR2 P38484 SMIM3 Homo sapiens Q9BZL3 32296183
Intra
IFNGR2 P38484 BNIP3 Homo sapiens Q12983 32296183
Intra
IFNGR2 P38484 UNC50 Homo sapiens Q53HI1 32296183
Intra
IFNGR2 P38484 INSIG2 Homo sapiens Q9Y5U4 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant IFNGR2 Proteins

Cat. No. Product Name Accession Purity
HY-P7367 IFN-gamma R2 Protein, Human (CHO) P38484 (S28-Q247) ≥95%

Related Diseases

Diseases Alias
Immunodeficiency 28

IMD28

Ifngr2 Deficiency

Immunodeficiency 28, Mycobacteriosis, Autosomal Recessive

Immunodeficiency 28, Mycobacteriosis

Mendelian Susceptibility To Mycobacterial Diseases Due To Complete Ifngammar2 Deficiency

Mendelian Susceptibility To Mycobacterial Diseases Due To Complete Interferon Gamma Receptor 2 Deficiency

Msmd Due To Complete Ifngammar2 Deficiency

Msmd Due To Complete Interferon Gamma Receptor 2 Deficiency

Autosomal Recessive Mendelian Susceptibility To Mycobacterial Diseases Due To Partial Ifngammar2 Deficiency

Autosomal Recessive Msmd Due To Partial Ifngammar2 Deficiency

Autosomal Recessive Msmd Due To Partial Interferon Gamma Receptor 2 Deficiency

Autosomal Recessive Mendelian Susceptibility To Mycobacterial Diseases Due To Partial Interferon Gamma Receptor 2 Deficiency

Immunodeficiency, Type 28, Mycobacteriosis

Autosomal Dominant Mendelian Susceptibility To Mycobacterial Diseases Due To Partial Ifngammar2 Deficiency

Autosomal Dominant Msmd Due To Partial Ifngammar2 Deficiency

Autosomal Dominant Msmd Due To Partial Interferon Gamma Receptor 2 Deficiency

Autosomal Dominant Mendelian Susceptibility To Mycobacterial Diseases Due To Partial Interferon Gamma Receptor 2 Deficiency

Mycobacterium Abscessus
Tuberculous Salpingitis
Axillary Adenitis

Axillary Lymphadenitis

Immunodeficiency 27b

Autosomal Dominant Mendelian Susceptibility To Mycobacterial Diseases Due To Partial Ifngammar1 Deficiency

IMD27B

Immunodeficiency 27b, Mycobacteriosis, Autosomal Dominant

Ifngr1 Deficiency, Autosomal Dominant

Autosomal Dominant Mendelian Susceptibility To Mycobacterial Diseases Due To Partial Interferon Gamma Receptor 1 Deficiency

Autosomal Dominant Msmd Due To Partial Ifngammar1 Deficiency

Autosomal Dominant Msmd Due To Partial Interferon Gamma Receptor 1 Deficiency

Immunodeficiency 27b, Mycobacteriosis, Ad

Autosomal Dominant Ifngr1 Deficiency

Autosomal Dominant Immunodeficiency 27b, Mycobacteriosis

Immunodeficiency, Type 27b, Mycobacteriosis, Autosomal Dominant

Lepromatous Leprosy

Leprosy, Lepromatous

Type L Leprosy

Leprosy Lepromatous

Aneurysm, Intracranial Berry, 12

ANIB12

Intracranial Berry Aneurysm 12

Sezary'S Disease

Sezary Syndrome

Sézary Syndrome

Sezary'S Lymphoma

Sezary Disease

Sezary Erythroderma

Sezary Lymphoma

Silo Filler'S Disease

Silo Filler Disease

Silo-Fillers' Disease

Opportunistic Bacterial Infectious Disease
Nocardiosis

Nocardia Infection

Nocardia Infections

Nocardia Infectious Disease

Lung Nocardiosis

Nocardiasis

Nocardiosis Nos

Macs Syndrome

Macrocephaly, Alopecia, Cutis Laxa, And Scoliosis

Mycobacterium Avium Complex Disease

Rin2 Syndrome

Mycobacterium Avium-Intracellulare Infection

Tall Forehead, Sparse Hair, Skin Hyperextensibility, And Scoliosis

Mycobacterium Avium Complex

Mycobacterium Avium Infection

Infection Due To Mycobacterium Intracellulare

Mac Disease

Macrocephaly-Alopecia-Cutis Laxa-Scoliosis Syndrome

Rin2 Deficiency

Tall Forehead-Sparse Hair-Skin Hyperextensibility-Scoliosis Syndrome

MACS

Macrocephaly Alopecia Cutis Laxa And Scoliosis Syndrome

Immunodeficiency 21

Monocytopenia And Mycobacterial Infection Syndrome

Monomac

Gata2 Deficiency

Monocytopenia With Susceptibility To Infections

Dcml

IMD21

Dendritic Cell, Monocyte, B Lymphocyte, And Natural Killer Lymphocyte Deficiency

Monocytopenia With Susceptibility To Mycobacterial, Fungal, And Papillomavirus Infections And Myelodysplasia

Combined Immunodeficiency With Susceptibility To Mycobacterial, Viral, And Fungal Infections

Combined Immunodeficiency With Susceptibility To Mycobacterial, Viral And Fungal Infections

Dendritic Cell, Monocyte, B And Nk Lymphoid Deficiency

Monocyte-B-Natural Killer-Dendritic Cell Deficiency Syndrome

Monocytopenia With Mycobacterial, Fungal, And Papillomavirus Infections And Myelodysplasia

Combined Immunodeficiency With Mycobacterial, Viral, And Fungal Infections

Monocyte - B - Natural Killer - Dendritic Cell Deficiency

Combined Immunodeficiency With Susceptibility To Mycobacterial Viral And Fungal Infections

Dendritic Cell Monocyte Lymphocyte B And Natural Killer Lymphocyte Deficiency

Monocytopenia With Susceptibility To Mycobacterial Fungal And Papillomavirus Infections And Myelodysplasia

Sarcoidosis 1

Sarcoidosis

Boeck Sarcoid

Besnier-Boeck-Schaumann Disease

SS1

Sarcoidosis, Susceptibility To, 1

Lymphogranulomatosis

Hodgkin Disease

Boeck'S Disease

Boeck'S Sarcoid

Schaumann'S Disease Or Syndrome

Hutchinson-Boeck Disease Or Syndrome

Immunodeficiency 27a

IMD27A

Autosomal Recessive Ifngr1 Deficiency

Autosomal Recessive Immunodeficiency 27a, Mycobacteriosis

Autosomal Recessive Mendelian Susceptibility To Mycobacterial Diseases Due To Partial Ifngammar1 Deficiency

Autosomal Recessive Mendelian Susceptibility To Mycobacterial Diseases Due To Partial Interferon Gamma Receptor 1 Deficiency

Autosomal Recessive Msmd Due To Partial Ifngammar1 Deficiency

Autosomal Recessive Msmd Due To Partial Interferon Gamma Receptor 1 Deficiency

Immunodeficiency 27a, Mycobacteriosis, Autosomal Recessive

Ifngr1 Deficiency, Autosomal Recessive

Immunodeficiency 27a, Mycobacteriosis, Ar

Mendelian Susceptibility To Mycobacterial Diseases Due To Complete Ifngammar1 Deficiency

Msmd Due To Complete Ifngammar1 Deficiency

Msmd Due To Complete Interferon Gamma Receptor 1 Deficiency

Mendelian Susceptibility To Mycobacterial Diseases Due To Complete Interferon Gamma Receptor 1 Deficiency

Familial Disseminated Atypical Mycobacterial Infection

Interferon Gamma, Receptor 1, Deficiency

Immunodeficiency, Type 27a, Mycobacteriosis, Ar

Mycobacterial Disease, Mendelian Susceptibility To

Chronic Mucocutaneous Candidiasis

Candidiasis, Chronic Mucocutaneous

Cmc

Candidiasis Chronic Mucocutaneous

Asthma

Chronic Obstructive Asthma

Asthma, Diminished Response To Antileukotriene Treatment In

Bronchial Hyperreactivity

Asthma, Susceptibility To

Asthma, Bronchial

Asthma, Protection Against

Asthma, Nocturnal, Susceptibility To

Nocturnal Asthma

Asthma-Related Traits

Asthma-Related Traits, Susceptibility To

Asthma, Nocturnal

Chronic Obstructive Asthma With Acute Exacerbation

Chronic Obstructive Asthma With Status Asthmaticus

Exercise Induced Asthma

Exercise-Induced Asthma

Bronchial Asthma

Asthma, Exercise-Induced

Idiosyncratic Asthma

Unspecified Asthma With Acute Exacerbation

Asthma, Unspecified, With Stated Status Asthmaticus

Status Asthmaticus Nos

Acute Severe Asthma

Acute Severe Bronchial Asthma

Status Asthma

Status Post Asthmaticus

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]

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 IFNGR2 RGD RGD:1307532
Macaca mulatta IFNGR2 VGNC VGNC:73569
Felis catus IFNGR2 VGNC VGNC:67706
Bos taurus IFNGR2 VGNC VGNC:30059
Mus musculus IFNGR2 MGD MGI:107654
Others IFNGR2 NCBI