1. Gene
  2. IRF2BP2 - interferon regulatory factor 2 binding protein 2 Gene

IRF2BP2 - interferon regulatory factor 2 binding protein 2 Gene

Homo sapiens

Also known as CVID14

Gene ID: 359948 | Gene type: protein coding

About IRF2BP2

Cytogenetic location: 1q42.3 Genomic coordinates (GRCh38): 1:234,604,269-234,610,178 (from NCBI)

This gene has 3 transcripts (splice variants), 260 orthologues, 5 paralogues and is associated with 3 phenotypes. Ubiquitous expression in bone marrow (RPKM 91.3), thyroid (RPKM 43.5) and 25 other tissues.

Summary

This gene encodes an interferon regulatory factor-2 (IRF2) binding protein that interacts with the C-terminal transcriptional repression domain of IRF2. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]

IRF2BP2 Products(2)

mRNA Protein Name
NM_001077397.1 NP_001070865.1 interferon regulatory factor 2-binding protein 2 isoform B
NM_182972.3 NP_892017.2 interferon regulatory factor 2-binding protein 2 isoform A

IRF2BP2 Protein Structure

IRF-2BP1_2

IRF-2BP1_2: Interferon regulatory factor 2-binding protein zinc finger (11 - 64)

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  • 587 a.a.
Protein Preferred Names Protein Names

interferon regulatory factor 2-binding protein 2

IRF-2-binding protein 2

Related Diseases

Diseases Alias
Immunodeficiency, Common Variable, 14

CVID14

Common Variable Immunodeficiency 14

Common Variable Immunodeficiency

Cvid

Common Variable Agammaglobulinemia

Common Variable Immune Deficiency

Acquired Hypogammaglobulinemia

Hypogamma-Globulinemia, Acquired

Idiopathic Immunoglobulin Deficiency

Primary Antibody Deficiency

Primary Hypogammaglobulinemia

Acquired Agammaglobulinemia

Sporadic Hypogammaglobulinemia

Common Variable Hypogamma-Globulinemia

Immunoglobulin Deficiency, Late-Onset

Common Variable Hypogammaglobulinemia

Immunodeficiency, Common Variable

Acute Promyelocytic Leukemia

Leukemia, Acute Promyelocytic

Acute Myeloblastic Leukemia Type 3

Aml M3

APL

Leukemia, Acute Promyelocytic, Somatic

Aml With T(15

17)(Q22

Q12)

(Pml/Raralpha) And Variants

Apml

Acute Myeloblastic Leukemia 3

Acute Myeloid Leukemia With T(15

17)(Q22

Q12)

(Pml/Raralpha) And Variants

Acute Myeloblastic Leukaemia Type 3

Acute Myeloid Leukaemia M3

Acute Myeloid Leukemia M3

Acute Promyelocytic Leukaemia

M3 Anll

Myeloid Leukemia, Acute, M3

Leukemia Promyelocytic Acute

Leukemia, Promyelocytic, Acute

Leukemia, Acute, Promyelocytic

Mesenchymal Chondrosarcoma

Chondrosarcoma, Mesenchymal

Chondrosarcoma Mesenchymal

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
Mus musculus IRF2BP2 MGD MGI:2443921
Rattus norvegicus IRF2BP2 RGD RGD:1589517
Bos taurus IRF2BP2 VGNC VGNC:30272
Canis familiaris IRF2BP2 VGNC VGNC:51901
Macaca mulatta IRF2BP2 VGNC VGNC:106391