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10 sources retrieved · Most recent: April 2026 · Index updated 15 days ago
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GBP7
guanylate binding protein 7
Chromosome 1 · 1p22.2
NCBI Gene: 388646Ensembl: ENSG00000213512.4HGNC: HGNC:29606UniProt: Q8N8V2
11PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
regulation of canonical NF-kappaB signal transductionpositive regulation of viral genome replicationnegative regulation of receptor signaling pathway via JAK-STATnegative regulation of type I interferon productionImmunodeficiency due to a late component of complements deficiencyChronic mucocutaneous candidosisrecurrent Neisseria infections due to factor D deficiencyimmunodeficiency 28
✦AI Summary

GBP7 is an interferon-inducible GTPase that exhibits context-dependent functions in host immunity. As a member of the guanylate binding protein family, GBP7 hydrolyzes GTP to GDP and GMP with high affinity (KD = 0.22 µM) and demonstrates concentration-dependent GTPase activity 1. The protein forms transient dimers and possesses an elongated C-terminal tail that is required for recruitment to pathogen-containing vacuoles 1. Evolutionarily, GBP7 emerged from GBP4 duplication and appears exclusive to primates 2. Functionally, GBP7 plays opposing roles depending on the pathogen. Against bacterial infections like Brucella abortus, GBP7 contributes to inflammasome activation and pathogen control through cooperation with other GBPs 3. However, during influenza A virus infection, GBP7 facilitates viral replication by suppressing innate immune responses through inhibition of NF-κB and JAK-STAT signaling pathways, leading to reduced type I and III interferon production 4. GBP7 expression is upregulated during various infections including chikungunya virus in the central nervous system 5. In cancer contexts, GBP7 shows variable prognostic significance, with low expression associated with shorter overall survival in head and neck squamous cell carcinoma 6. This dual functionality highlights GBP7's complex role in immunity and disease.

Sources cited
1
GBP7 biochemical properties including GTPase activity, GTP binding affinity, dimer formation, and C-terminal tail function
PMID: 31689351
2
Evolutionary origin of GBP7 from GBP4 duplication and primate-specific presence
PMID: 33550067
3
Role in bacterial infection control and inflammasome activation through GBP cooperation
PMID: 38404575
4
Facilitation of influenza A virus replication through suppression of innate immunity via NF-κB and JAK-STAT pathways
PMID: 33408175
5
Upregulation during chikungunya virus infection in central nervous system
PMID: 29067635
6
Prognostic significance in head and neck squamous cell carcinoma
PMID: 32269280
Disease Associationsⓘ20
Immunodeficiency due to a late component of complements deficiencyOpen Targets
0.10Suggestive
Chronic mucocutaneous candidosisOpen Targets
0.07Suggestive
recurrent Neisseria infections due to factor D deficiencyOpen Targets
0.07Suggestive
immunodeficiency 28Open Targets
0.07Suggestive
Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiencyOpen Targets
0.07Suggestive
varicella, severe recurrentOpen Targets
0.07Suggestive
candidiasis, familial, 4Open Targets
0.06Suggestive
isolated asymptomatic elevation of creatine phosphokinaseOpen Targets
0.06Suggestive
immunodeficiency 31BOpen Targets
0.06Suggestive
Susceptibility to viral and mycobacterial infectionsOpen Targets
0.06Suggestive
type II complement component 8 deficiencyOpen Targets
0.06Suggestive
Autosomal recessive hyper-IgE syndromeOpen Targets
0.06Suggestive
Autosomal recessive hyper-IgE syndrome due to TYK2 deficiencyOpen Targets
0.06Suggestive
immunodeficiency 35Open Targets
0.06Suggestive
mannose-binding lectin deficiencyOpen Targets
0.06Suggestive
Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiencyOpen Targets
0.05Suggestive
immunodeficiency due to ficolin3 deficiencyOpen Targets
0.05Suggestive
pentosuriaOpen Targets
0.04Suggestive
Immunodeficiency due to a complement cascade protein anomalyOpen Targets
0.04Suggestive
autosomal recessive severe congenital neutropenia due to JAGN1 deficiencyOpen Targets
0.04Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
ATG4BProtein interaction73%GBP2Shared pathway33%GBP6Shared pathway33%GBP4Shared pathway27%GBP3Shared pathway20%PDE12Shared pathway19%
Tissue Expression6 tissues
Liver
100%
Lung
0%
Brain
0%
Ovary
0%
Bone Marrow
0%
Heart
0%
Gene Interaction Network
Click a node to explore
GBP7ATG4BGBP2GBP6GBP4GBP3PDE12
PROTEIN STRUCTURE
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AlphaFoldAI-predicted · UniProt Q8N8V2
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
0.87LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF0.66 [0.51–0.87]
RankingsWhere GBP7 stands among ~20K protein-coding genes
  • #16,762of 20,598
    Most Researched11
  • #7,645of 17,882
    Most Constrained (LOEUF)0.87
Genes detectedGBP7
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Evolution of the guanylate binding protein (GBP) genes: Emergence of GBP7 genes in primates and further acquisition of a unique GBP3 gene in simians.
PMID: 33550067
Mol Immunol · 2021
1.00
2
Multifaceted Roles of Guanylate-Binding Proteins in Cancer.
PMID: 40564939
Int J Mol Sci · 2025
0.90
3
Biochemical and structural characterization of murine GBP7, a guanylate binding protein with an elongated C-terminal tail.
PMID: 31689351
Biochem J · 2019
0.80
4
Inducible Guanylate-Binding Protein 7 Facilitates Influenza A Virus Replication by Suppressing Innate Immunity via NF-κB and JAK-STAT Signaling Pathways.
PMID: 33408175
J Virol · 2021
0.70
5
Microneedle-mediated delivery of hydroxypropyl-β-cyclodextrin-encapsulated Angelica sinensis (Danggui) essential oil for acne treatment: efficacy and mechanisms.
PMID: 40883577
Drug Deliv Transl Res · 2026
0.60