| Primary Identifier | MGI:96395 | Organism | mouse, laboratory |
| Chromosome | 8 | NCBI Gene Number | 15900 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0) Enables RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Involved in mononuclear cell differentiation and regulation of gene expression. Acts upstream of or within several processes, including defense response to protozoan; positive regulation of macromolecule biosynthetic process; and response to bacterium. Located in nucleus. Is expressed in several structures, including central nervous system; genitourinary system; hemolymphoid system; intestine; and lens. Used to study familial chronic myelocytic leukemia-like syndrome. Human ortholog(s) of this gene implicated in Behcet's disease; immunodeficiency 32A; immunodeficiency 32B; multiple myeloma; and systemic lupus erythematosus. Orthologous to human IRF8 (interferon regulatory factor 8). PHENOTYPE: Homozygotes for a targeted null mutation exhibit increased incidence of viral infections, shortened life span, deregulated hematopoiesis, and hematological neoplasias. Heterozygotes show similar, but milder, phenotypes. [provided by MGI curators] |
Features --> Cross References
Canonical gene --> CDSs in specific strains.
Canonical gene --> Exons in specific strains
Canonical gene --> Strain-specific IDs, biotypes, and locations
Canonical gene --> Transcripts in specific strains.
Features --> Overlapping features
