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UNC93B1

Function

Plays an important role in innate and adaptive immunity by regulating nucleotide-sensing Toll-like receptor (TLR) signaling. Required for the transport of a subset of TLRs (including TLR3, TLR7 and TLR9) from the endoplasmic reticulum to endolysosomes where they can engage pathogen nucleotides and activate signaling cascades. May play a role in autoreactive B-cells removal.

Involvement in disease

Encephalopathy, acute, infection-induced, 1, herpes-specific

IIAE1

A rare complication of human herpesvirus 1 (HHV-1) infection, occurring in only a small minority of HHV-1 infected individuals. It is characterized by hemorrhagic necrosis of parts of the temporal and frontal lobes. Onset is over several days and involves fever, headache, seizures, stupor, and often coma, frequently with a fatal outcome.

None

Disease susceptibility is associated with variants affecting the gene represented in this entry. Mutations in UNC93B1 resulting in autosomal recessive UNC93B1 deficiency predispose otherwise healthy individuals to isolated herpes simplex encephalitis due to impaired IFNs production. UNC93B1 deficiency, however, does not compromise immunity to most pathogens, unlike most known primary immunodeficiencies.

Post-translational modifications

N-glycosylated.

Sequence Similarities

Belongs to the unc-93 family.

Tissue Specificity

Expressed in plasmocytoid dendritic cells (at protein level). Highly expressed in antigen-presenting cells. Expressed in heart, and at lower level in kidney. Expressed at low level in other tissues.

Cellular localization

Alternative names

UNC93, UNC93B, UNC93B1, Protein unc-93 homolog B1, Unc-93B1, hUNC93B1

swissprot:Q9H1C4 entrezGene:81622 omim:608204