IL10RB - interleukin 10 receptor subunit beta Gene

Also Known as CRFB4; CRF2-4; D21S58; D21S66; CDW210B; IL-10R2; IL-10RB

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 3588

About IL10RB

Cytogenetic location: 21q22.11 Genomic coordinates (GRCh38): 21:33,266,367-33,297,221 (from NCBI)

This gene has 9 transcripts (splice variants), 210 orthologues, 11 paralogues and is associated with 3 phenotypes. Ubiquitous expression in placenta (RPKM 32.9), colon (RPKM 23.4) and 25 other tissues.

Summary

The protein encoded by this gene belongs to the cytokine receptor family. It is an accessory chain essential for the active interleukin 10 receptor complex. Coexpression of this and IL10RA proteins has been shown to be required for IL10-induced signal transduction. This gene and three Other interferon receptor genes, IFAR2, IFNAR1, and IFNGR2, form a class II cytokine receptor gene cluster located in a small region on chromosome 21. [provided by RefSeq, Jul 2008]

IL10RB Products (4)

mRNA Protein Name
NM_000628.5 NP_000619.3 interleukin-10 receptor subunit beta isoform 1 precursor
NM_001405849.1 NP_001392778.1 interleukin-10 receptor subunit beta isoform 2 precursor
NM_001405850.1 NP_001392779.1 interleukin-10 receptor subunit beta isoform 3 precursor
NM_001406840.1 NP_001393769.1 interleukin-10 receptor subunit beta isoform 4 precursor
Molecular Function GO Annotation Evidence References Source
enables coreceptor activity IDA
IDA: Inferred from direct assay
16982608 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
12483210 GOA
Biological Process GO Annotation Evidence References Source
involved in interleukin-10-mediated signaling pathway IDA
IDA: Inferred from direct assay
16982608 GOA
involved in positive regulation of cellular respiration IMP
IMP: Inferred from mutant phenotype
25930096 GOA
involved in positive regulation of receptor signaling pathway via JAK-STAT IDA
IDA: Inferred from direct assay
16982608 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

IL10RB Protein Structure

Tissue_fac

Tissue_fac: Tissue factor (13 - 100)

Interfer-bind

Interfer-bind: Interferon-alpha/beta receptor, fibronectin type III (111 - 213)

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

interleukin-10 receptor subunit beta

  • IL-10 receptor subunit beta

IL10RB Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
IL10RB Q08334 IL22RA1 Homo sapiens Q8N6P7 15120653
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant IL10RB Proteins

Cat. No. Product Name Accession Purity
HY-P72599 IL-10R beta Protein, Human (HEK293, His) Q08334/NP_000619.3 (M20-S220) ≥ 95%, as determined by reducing SDS-PAGE.
HY-P74839 IL-10R beta Protein, Human (HEK293, His-hFc) Q08334 (M20-S220) ≥ 90%, as determined by reducing SDS-PAGE.

IL10RB Antibodies

Cat. No. Product Name Application Reactivity
HY-P84509 IL10RB Antibody (YA4206) WB, FC, ELISA Human, Rat
HY-P84509A IL10RB Antibody (YA4206)(PBS only) WB, FC, ELISA Human, Rat
HY-P84510 IL10RB Antibody (YA4207) ICC/IF, FC, ELISA Human
HY-P84510A IL10RB Antibody (YA4207)(PBS only) ICC/IF, FC, ELISA Human

Related Diseases

Diseases Alias
Inflammatory Bowel Disease 25, Autosomal Recessive
  • Immune Dysregulation-Inflammatory Bowel Disease-Arthritis-Recurrent Infections Syndrome

  • IBD25

  • Inflammatory Bowel Disease 25, Early Onset, Autosomal Recessive

  • Il10-Related Early-Onset Ibd

  • Il10-Related Early-Onset Inflammatory Bowel Disease

  • Inflammatory Bowel Disease, Early-Onset, Autosomal Recessive

  • Autosomal Recessive Early-Onset Inflammatory Bowel Disease

  • Autosomal Recessive Early-Onset Ibd

  • Early-Onset Autosomal Recessive Inflammatory Bowel Disease

  • Bowel Disease, Inflammatory, Type 25, Autosomal Recessive

Inflammatory Bowel Disease 25
  • Early Onset Autosomal Recessive Inflammatory Bowel Disease 25

  • Ibd25

  • Inflammatory Bowel Disease 25, Autosomal Recessive

Hepatitis B
  • Chronic Hepatitis B

  • Hepatitis B Infection

  • Serum Hepatitis

  • HBV

  • Hepatitis B Chronic

  • Hbv, Susceptibility To

  • Hepatitis B, Chronic

  • Chronic Hepatitis B Without Delta Agent

  • Chronic Hbv - [Hepatitis B Virus] Infection

  • Hepatitis B Nos

  • Chronic Type B Viral Hepatitis

  • Hep B Nos

Colitis
Ulcerative Colitis
  • Colitis Gravis

  • Left Sided Ulcerative Colitis

  • Left-Sided Ulcerative Colitis

  • Idiopathic Proctocolitis

  • Inflammatory Bowel Disease, Ulcerative Colitis Type

  • Uc

  • Colitis Ulcerative

  • Colitis, Ulcerative

  • Chronic Left-Sided Ulcerative Colitis

  • Uc - [Ulcerative Colitis]

  • Chronic Ulcerative Enteritis

  • Mucosal Proctocolitis

  • Ulcerative Mucosal Proctocolitis

  • Left Hemicolitis

Erythematosquamous Dermatosis
  • Other Erythematosquamous Dermatosis

Inflammatory Bowel Disease
  • Inflammatory Bowel Diseases

  • Bowel Disease, Inflammatory

Rubella
  • German Measles

  • Three Day Measles

  • Rubella Nos

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

Folliculitis
Narcolepsy
  • Paroxysmal Sleep

  • Gelineau Syndrome

  • Narcoleptic Syndrome

  • Narcolepsy-Cataplexy Syndrome

  • Cataplexy And Narcolepsy

  • Narcolepsy, Without Cataplexy

  • Gelineau'S Syndrome

  • Narcolepsy With Or Without Cataplexy

  • Narcolepsy Nos

Immunodeficiency 35
  • Tyrosine Kinase 2 Deficiency

  • IMD35

  • Tyk2 Deficiency

  • Autosomal Recessive Hyper-Ige Syndrome With Atypical Mycobacteriosis

  • Susceptibility To Infection Due To Tyk2 Deficiency

  • Hyper-Ige Syndrome With Atypical Mycobacteriosis, Autosomal Recessive

  • Hies With Atypical Mycobacteriosis, Autosomal Recessive

  • Autosomal Recessiv Hies With Atypical Mycobacteriosis

  • Autosomal Recessive Hyper-Ige Syndrome Due To Tyk2 Deficiency

  • Autosomal Recessive Hies With Atypical Mycobacteriosis

Acute Necrotizing Encephalitis
  • Acute Necrotizing Encephalopathy

  • Postinfectious Acute Necrotizing Hemorrhagic Encephalopathy

  • Ane

  • Acute Necrotizing Encephalopathy Type 1

  • Adane

  • Ane1

  • Autosomal Dominant Acute Necrotizing Encephalopathy

  • Iiae3

  • Susceptibility To Acute Necrotizing Encephalopathy

  • Susceptibility To Infection-Induced Acute Encephalopathy

  • Encephalopathy, Acute Necrotizing, Susceptibility To

  • Encephalitis, Acute Necrotizing

Gastrointestinal Defects And Immunodeficiency Syndrome 1
  • Familial Intestinal Polyatresia Syndrome

  • Fipa

  • Gastrointestinal Defects And Immunodeficiency Syndrome

  • Multiple Gastrointestinal Atresias

  • Familial Isolated Pituitary Adenoma

  • Intestinal Atresia, Multiple

  • Multiple Intestinal Atresia

  • GIDID1

  • Multiple Intestinal Atresia And/Or Inflammatory Bowel Disease With Or Without Immunodeficiency

  • Minat

  • Gidid

  • Meddra:10028210

  • Familial Isolated Pituitary Adenoma Syndrome

  • Intestinal Atresia Multiple

  • Combined Immunodeficiency-Enteropathy Spectrum

  • Cid-Mia/Early-Onset Ibd

  • Intestinal Atresia, Multiple And/Or Inflammatory Bowel Disease With Or Without Immunodeficiency

  • Mia

  • Gastrointestinal Defect And Immunodeficiency Syndrome

  • Pituitary Adenoma Predisposition

  • Pituitary Adenoma, Familial Isolated

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 IL10RB RGD RGD:1560373
Bos taurus IL10RB VGNC VGNC:56219
Felis catus IL10RB VGNC VGNC:97463
Mus musculus IL10RB MGD MGI:109380
Others IL10RB NCBI