UNC93B1 - unc-93 homolog B1, TLR signaling regulator Gene

Also Known as IIAE1; UNC93; UNC93B; Unc-93B1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 81622

About UNC93B1

Cytogenetic location: 11q13.2 Genomic coordinates (GRCh38): 11:67,991,100-68,004,097 (from NCBI)

This gene has 9 transcripts (splice variants), 223 orthologues, 1 paralogue and is associated with 2 phenotypes. Broad expression in spleen (RPKM 27.3), lung (RPKM 14.0) and 24 other tissues.

Summary

This gene encodes a protein that is involved in innate and adaptive immune response by regulating Toll-like Receptor signaling. The encoded protein traffics nucleotide sensing toll-like receptors to the endolysosome from the endoplasmic reticulum. Deficiency of the encoded protein has been associated with herpes simplex encephalitis. [provided by RefSeq, Feb 2014]

UNC93B1 Products (1)

mRNA Protein Name
NM_030930.4 NP_112192.2 protein unc-93 homolog B1
Molecular Function GO Annotation Evidence Références Source
enables Toll-like receptor binding IPI
IPI: Inferred from physical interaction
33432245 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
22164301 GOA
Biological Process GO Annotation Evidence Références Source
involved in toll-like receptor 3 signaling pathway IMP
IMP: Inferred from mutant phenotype
18082565 GOA
involved in toll-like receptor 7 signaling pathway IMP
IMP: Inferred from mutant phenotype
19006693 GOA
involved in toll-like receptor 9 signaling pathway IMP
IMP: Inferred from mutant phenotype
19006693 GOA
Cellular Component GO Annotation Evidence Références Source
located in endoplasmic reticulum IDA
IDA: Inferred from direct assay
18082565 GOA
located in endosome IDA
IDA: Inferred from direct assay
21642595 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

UNC93B1 Protein Structure

UNC-93

UNC-93: Ion channel regulatory protein UNC-93 (122 - 188)

  • 0
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  • 200
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  • 400
  • 500
  • 596 a.a.
Protein Preferred Names Protein Names

protein unc-93 homolog B1

  • unc-93 related protein

UNC93B1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Références
Intra
UNC93B1 Q9H1C4 LDLRAD1 Homo sapiens Q5T700 32296183
Intra
UNC93B1 Q9H1C4 LDLRAD1 Homo sapiens Q5T700 32296183
Intra
UNC93B1 Q9H1C4 TMEM237 Homo sapiens Q96Q45-2 32296183
Intra
UNC93B1 Q9H1C4 TMEM237 Homo sapiens Q96Q45-2 32296183
Intra
UNC93B1 Q9H1C4 MFF Homo sapiens Q9GZY8-5 32296183
Intra
UNC93B1 Q9H1C4 MFF Homo sapiens Q9GZY8-5 32296183
Intra
UNC93B1 Q9H1C4 GPRC5D Homo sapiens Q9NZD1 32296183
Intra
UNC93B1 Q9H1C4 GPRC5D Homo sapiens Q9NZD1 32296183
Intra
UNC93B1 Q9H1C4 GPRC5D Homo sapiens Q9NZD1 32296183
Intra
UNC93B1 Q9H1C4 TM4SF18 Homo sapiens Q96CE8 32296183
Intra
UNC93B1 Q9H1C4 TM4SF18 Homo sapiens Q96CE8 32296183
Intra
UNC93B1 Q9H1C4 REEP1 Homo sapiens Q9H902 32296183
Intra
UNC93B1 Q9H1C4 REEP1 Homo sapiens Q9H902 32296183
Intra
UNC93B1 Q9H1C4 REEP1 Homo sapiens Q9H902 32296183
Intra
UNC93B1 Q9H1C4 SSMEM1 Homo sapiens Q8WWF3 32296183
Intra
UNC93B1 Q9H1C4 SSMEM1 Homo sapiens Q8WWF3 32296183
Intra
UNC93B1 Q9H1C4 SLC35C2 Homo sapiens Q9NQQ7-3 32296183
Intra
UNC93B1 Q9H1C4 SLC35C2 Homo sapiens Q9NQQ7-3 32296183
Intra
UNC93B1 Q9H1C4 SLC35C2 Homo sapiens Q9NQQ7-3 32296183
Intra
UNC93B1 Q9H1C4 LEUTX Homo sapiens A8MZ59 32296183
Intra
UNC93B1 Q9H1C4 LEUTX Homo sapiens A8MZ59 32296183
Intra
UNC93B1 Q9H1C4 FFAR3 Homo sapiens O14843 32296183
Intra
UNC93B1 Q9H1C4 FFAR3 Homo sapiens O14843 32296183
Intra
UNC93B1 Q9H1C4 GPR101 Homo sapiens Q96P66 32296183
Intra
UNC93B1 Q9H1C4 GPR101 Homo sapiens Q96P66 32296183
Intra
UNC93B1 Q9H1C4 BEST2 Homo sapiens Q8NFU1 32296183
Intra
UNC93B1 Q9H1C4 BEST2 Homo sapiens Q8NFU1 32296183
Cross
UNC93B1 Q9H1C4 ns7b_sars2 SARS-CoV-2 P0DTD8 33845483
Intra
UNC93B1 Q9H1C4 LIME1 Homo sapiens Q9H400 32296183
Intra
UNC93B1 Q9H1C4 LIME1 Homo sapiens Q9H400 32296183
Intra
UNC93B1 Q9H1C4 LIME1 Homo sapiens Q9H400 32296183
Intra
UNC93B1 Q9H1C4 CSE1L Homo sapiens P55060 30833792
Intra
UNC93B1 Q9H1C4 KPNB1 Homo sapiens Q14974 30833792
Intra
UNC93B1 Q9H1C4 HHLA2 Homo sapiens Q9UM44 32296183
Intra
UNC93B1 Q9H1C4 HHLA2 Homo sapiens Q9UM44 32296183
Intra
UNC93B1 Q9H1C4 HHLA2 Homo sapiens Q9UM44 32296183
Intra
UNC93B1 Q9H1C4 GPR37L1 Homo sapiens O60883 32296183
Intra
UNC93B1 Q9H1C4 GPR37L1 Homo sapiens O60883 32296183
Intra
UNC93B1 Q9H1C4 EBP Homo sapiens Q15125 32296183
Intra
UNC93B1 Q9H1C4 EBP Homo sapiens Q15125 32296183
Intra
UNC93B1 Q9H1C4 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
UNC93B1 Q9H1C4 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
UNC93B1 Q9H1C4 SYNDIG1 Homo sapiens Q9H7V2 32296183
Intra
UNC93B1 Q9H1C4 SYNDIG1 Homo sapiens Q9H7V2 32296183
Intra
UNC93B1 Q9H1C4 SYNDIG1 Homo sapiens Q9H7V2 32296183
Intra
UNC93B1 Q9H1C4 CLDN7 Homo sapiens O95471 32296183
Intra
UNC93B1 Q9H1C4 CLDN7 Homo sapiens O95471 32296183
Intra
UNC93B1 Q9H1C4 FATE1 Homo sapiens Q969F0 32296183
Intra
UNC93B1 Q9H1C4 FATE1 Homo sapiens Q969F0 32296183
Intra
UNC93B1 Q9H1C4 CD79A Homo sapiens P11912 32296183
Intra
UNC93B1 Q9H1C4 CD79A Homo sapiens P11912 32296183
Intra
UNC93B1 Q9H1C4 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
UNC93B1 Q9H1C4 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
UNC93B1 Q9H1C4 ERGIC3 Homo sapiens Q9Y282 32296183
Intra
UNC93B1 Q9H1C4 KLRC1 Homo sapiens P26715 32296183
Intra
UNC93B1 Q9H1C4 KLRC1 Homo sapiens P26715 32296183
Intra
UNC93B1 Q9H1C4 CCDC107 Homo sapiens Q8WV48 32296183
Intra
UNC93B1 Q9H1C4 CCDC107 Homo sapiens Q8WV48 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Encephalopathy, Acute, Infection-Induced 1
  • Herpes Simplex Encephalitis, Susceptibility To, 1

  • IIAE1

  • Encephalopathy, Acute, Infection-Induced , Susceptibility To, 1

  • Herpes Simplex Encephalitis 1

  • Encephalopathy, Acute, Infection-Induced, 1, Herpes-Specific

  • Encephalopathy, Acute, Infection-Induced, 1

  • Hse1

  • Infection-Induced Acute Encephalopathy 1

Herpes Simplex Encephalitis
  • Hse

  • Hsv Encephalitis

  • Hsve

  • Herpes Simplex Meningo-Encephalitis

  • Herpes Simplex Neuroinvasion

  • Herpes Simplex Virus Encephalitis

  • Herpetic Encephalitis

  • Herpes Encephalitis

  • Herpes Simplex Virus 1 Encephalitis

Encephalitis
  • Mumps Encephalitis

  • Mumps Meningoencephalitis

  • Herpes Simplex Neuroinvasion

  • Herpetic Encephalitis

  • Herpetic Encephalopathy

  • Herpes Simplex Encephalitis, Myelitis Or Encephalomyelitis

  • Encephalitis Due To Herpesviridae

  • Encephalitis Due To Herpesvirus

  • Herpes Encephalitis

  • Herpesviral Encephalitis

  • Herpes Simplex Encephalitis

  • Hsv - [Herpes Simplex Virus] Encephalitis

  • Herpes Virus Encephalitis

  • Simian B Disease

  • Simian B Disorder

  • Encephalitis Nec

  • Idiopathic Encephalitis

Herpes Simplex
  • Herpes Simplex Infections

  • Herpesvirus Hominis Disease

  • Herpes Simplex Disease

  • Herpesviral Infection Due To Herpes Simplex

  • Infections Due To Simplex Virus

  • Herpes Nos

Melkersson-Rosenthal Syndrome
  • Melkersson Syndrome

  • Mros

  • Mrs

  • Cheilitis Granulomatosa Of Mescher-Melkersson-Rosenthal

  • Melkersson'S Syndrome

  • Cheilitis Granulomatosa

  • Granulomatous Cheilitis

Immunodeficiency 31b
  • IMD31B

  • Immunodeficiency 31b, Mycobacterial And Viral Infections, Autosomal Recessive

  • Autosomal Recessive Stat1 Deficiency

  • Predisposition To Severe Viral Infection Due To Stat1 Deficiency

  • Susceptibility To Viral And Mycobacterial Infections Due To Stat1 Deficiency

  • Stat1 Deficiency, Autosomal Recessive

  • Autosomal Recessive Immunodeficiency 31b, Mycobacterial And Viral Infections

  • Stat1 Deficiency

  • Autosomal Recessive Susceptibility To Mycobacterial And Viral Infections

  • Mycobacterial And Viral Infections Due To Complete Stat1 Deficiency

  • Immunodeficiency, Type 31b, Mycobacterial And Viral Infections, Autosomal Recessive

Viral Encephalitis
  • Epidemic Encephalitis

  • Encephalitis Viral

  • Encephalitis, Arbovirus

  • Arbovirus Encephalitis

  • Postviral Encephalitis Nos

  • Equine Encephalitis

  • Tick-Borne Encephalitis

  • Viral Encephalitis Transmitted By Tick

  • Mosquito-Borne Encephalitis

  • Acute Haemorrhagic Encephalitis

  • Acute Idiopathic Encephalitis

  • Chronic Viral Encephalitis

  • Endemic Encephalitis

  • Subacute Viral Encephalitis

  • Viral Haemorrhagic Encephalitis

  • Viral Nonepidemic Encephalitis

  • Nonepidemic Encephalitis

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

Hemophagocytic Lymphohistiocytosis, Familial, 2
  • Familial Hemophagocytic Lymphohistiocytosis 2

  • FHL2

  • Hplh2

  • Hlh2

  • Hemophagocytic Lymphohistiocytosis, Familial, 2, Susceptibility To

  • Lymphohistiocytosis, Hemophagocytic, Familial, Type 2

X-Linked Immunodeficiency 74
  • Immunodeficiency 74, Covid-19-Related, X-Linked

  • Imd74

  • Respiratory Insufficiency Due To Sars-Cov-2 Viral Infection

  • Tlr7 Deficiency

  • X-Linked Immunodeficiency 74,Covid-19-Related

Cataract 44
  • CTRCT44

  • Total Early-Onset Cataract

  • Cataract 44 And Hypotrichosis

  • Cataract And Hypotrichosis

  • Cataract, Type 44

Epidermodysplasia Verruciformis 1
  • Epidermodysplasia Verruciformis

  • Epidermodysplasia Verruciformis, Susceptibility To, 1

  • Lutz-Lewandowsky Epidermodysplasia Verruciformis

  • EV1

  • Lewandowsky-Lutz Syndrome

  • Ev

Aicardi-Goutieres Syndrome
  • Aicardi Goutieres Syndrome

  • Cree Encephalitis

  • Aicardi-Goutières Syndrome

  • Encephalopathy With Basal Ganglia Calcification

  • Ags

  • Encephalopathy With Intracranial Calcification And Chronic Lymphocytosis Of Cerebrospinal Fluid

  • Pseudotoxoplasmosis Syndrome

  • Encephalopathy, Familial Infantile, With Calcification Of Basal Ganglia And Chronic Cerebrospinal Fluid Lymphocytosis

  • Familial Infantile Encephalopathy With Intracranial Calcification And Chronic Cerebrospinal Fluid Lymphocytosis

  • Aicardi-Goutieres Syndrome 1

Amyotrophic Lateral Sclerosis 1
  • Amyotrophic Lateral Sclerosis

  • ALS

  • Lou Gehrig Disease

  • Amyotrophic Lateral Sclerosis Type 1

  • Charcot Disease

  • ALS1

  • Amyotrophic Lateral Sclerosis, Susceptibility To

  • Fals

  • Lou Gehrig'S Disease

  • Mnd

  • Motor Neuron Disease

  • Familial Amyotrophic Lateral Sclerosis

  • Amyotrophic Lateral Sclerosis 1, Familial

  • Amyotrophic Lateral Sclerosis 1, Autosomal Dominant

  • Motor Neuron Disease, Bulbar

  • Motor Neurone Disease

  • Amyotrophic Lateral Sclerosis With Dementia

  • Dementia With Amyotrophic Lateral Sclerosis

  • Motor Neuron Disease, Amyotrophic Lateral Sclerosis

  • Sclerosis, Lateral, Amyotrophic

  • Sclerosis, Lateral, Amyotrophic, Type 1

  • Amyotrophic Sclerosis

  • Als - [Amyotrophic Lateral Sclerosis]

  • Wasting Palsy

  • Amyotrophic Paralysis

  • Amyotrophy Lateral Sclerosis

  • Wasting Paralysis

  • Spinal Progressive Amyotrophy

  • Progressive Atrophic Paralysis

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 UNC93B1 MGD MGI:1859307
Canis familiaris UNC93B1 VGNC VGNC:49636
Macaca mulatta UNC93B1 VGNC VGNC:78927
Bos taurus UNC93B1 VGNC VGNC:49587
Felis catus UNC93B1 VGNC VGNC:66836
Rattus norvegicus UNC93B1 RGD RGD:1311984
Others UNC93B1 NCBI