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10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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RENBP
renin binding protein
Chromosome X · Xq28
NCBI Gene: 5973Ensembl: ENSG00000102032.14HGNC: HGNC:9959UniProt: P51606
37PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
N-acylglucosamine 2-epimerase activityextracellular exosomeprotein bindingpeptidase inhibitor activityrheumatoid arthritiscancerhepatocellular carcinomaneoplasm
✦AI Summary

RENBP (renin binding protein) is an X-chromosome X enzyme that catalyzes the interconversion of N-acetylglucosamine to N-acetylmannosamine, functioning as N-acylglucosamine 2-epimerase 123. It participates in the degradation pathway of N-glycolylneuraminic acid (Neu5Gc), a sialic acid present in food that humans cannot synthesize due to an inactive CMAH enzyme 3. RENBP is involved in regulating blood pressure and functions as an endopeptidase inhibitor 4. Genetically, RENBP variants have been associated with psychiatric disorders. A genome-wide association study identified SNP rs2269372 in RENBP at genome-wide significance for schizophrenia susceptibility in Han Chinese populations (P=3.98×10⁻⁸) 5. Systematic review of GWAS studies confirmed RENBP as a schizophrenia-associated locus 6. However, RENBP polymorphisms showed no direct association with essential hypertension in large-scale GWAS analyses 7. Recent studies reveal RENBP's clinical relevance in cancer immunotherapy and inflammatory disease. RENBP emerged as a prognostic biomarker in laryngeal cancer, with high-risk RENBP expression correlating with reduced CD8+ T cell infiltration and altered immunotherapy response 8. RENBP inhibition enhances metabolic glycoengineering efficiency in antigen-presenting cells, with 1.2-1.4 fold increases in vitro and >3-fold enhancement in B cells in vivo 4. Additionally, RENBP expression correlates with bronchopulmonary dysplasia severity in preterm infants 9.

Sources cited
1
RENBP catalyzes interconversion of N-acetylglucosamine to N-acetylmannosamine
PMID: 10502668
2
RENBP enzymatic function in N-acetylglucosamine-N-acetylmannosamine interconversion
PMID: 12499362
3
RENBP involved in Neu5Gc degradation pathway; humans lack CMAH enzyme for Neu5Gc synthesis
PMID: 9990133
4
SNP rs2269372 in RENBP achieves genome-wide significance for schizophrenia (P=3.98×10⁻⁸, OR=1.31)
PMID: 24043878
5
RENBP identified as schizophrenia-associated locus in systematic GWAS review
PMID: 31096178
6
RENBP polymorphisms show no direct association with hypertension in GWAS
PMID: 28425437
7
RENBP functions as prognostic biomarker in laryngeal cancer with immune implications
PMID: 40247837
8
RENBP inhibition enhances metabolic glycoengineering in APCs; RENBP functions as N-acylglucosamine 2-epimerase
PMID: 40780193
9
RENBP expression correlates with bronchopulmonary dysplasia severity in preterm infants
PMID: 35338351
Disease Associationsⓘ20
rheumatoid arthritisOpen Targets
0.17Weak
cancerOpen Targets
0.12Weak
hepatocellular carcinomaOpen Targets
0.12Weak
neoplasmOpen Targets
0.12Weak
breast cancerOpen Targets
0.11Weak
gliomaOpen Targets
0.11Weak
glioblastoma multiformeOpen Targets
0.11Weak
colorectal carcinomaOpen Targets
0.11Weak
Alzheimer diseaseOpen Targets
0.11Weak
infectionOpen Targets
0.10Weak
non-alcoholic fatty liver diseaseOpen Targets
0.10Weak
osteosarcomaOpen Targets
0.10Weak
chronic kidney diseaseOpen Targets
0.10Suggestive
nonpapillary renal cell carcinomaOpen Targets
0.10Suggestive
amyotrophic lateral sclerosisOpen Targets
0.10Suggestive
acute myeloid leukemiaOpen Targets
0.10Suggestive
bladder transitional cell carcinomaOpen Targets
0.10Suggestive
atherosclerosisOpen Targets
0.09Suggestive
type 2 diabetes mellitusOpen Targets
0.09Suggestive
heart failureOpen Targets
0.09Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
GNEProtein interaction99%NANSProtein interaction94%CHIAProtein interaction93%NAGKProtein interaction91%CHIT1Protein interaction90%HEXAProtein interaction90%
Tissue Expression6 tissues
Lung
100%
Bone Marrow
51%
Heart
40%
Brain
32%
Liver
18%
Ovary
6%
Gene Interaction Network
Click a node to explore
RENBPGNENANSCHIANAGKCHIT1HEXA
PROTEIN STRUCTURE
Preparing viewer…
AlphaFoldAI-predicted · UniProt P51606
View on AlphaFold ↗
Constraintⓘ
LOEUFⓘ
0.64LoF Tolerant
pLIⓘ
0.19Tolerant
Observed/Expected LoF0.42 [0.29–0.64]
RankingsWhere RENBP stands among ~20K protein-coding genes
  • #10,679of 20,598
    Most Researched37
  • #4,616of 17,882
    Most Constrained (LOEUF)0.64
Genes detectedRENBP
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Prognostic value and immunotherapy analysis of immune cell-related genes in laryngeal cancer.
PMID: 40247837
PeerJ · 2025
1.00
2
Common variants on Xq28 conferring risk of schizophrenia in Han Chinese.
PMID: 24043878
Schizophr Bull · 2014
0.90
3
Are genetic polymorphisms in the renin-angiotensin-aldosterone system associated with essential hypertension? Evidence from genome-wide association studies.
PMID: 28425437
J Hum Hypertens · 2017
0.80
4
The human renin-binding protein gene (RENBP) maps in Xq28.
PMID: 8088804
Genomics · 1994
0.70
5
Unravelling the genetic basis of schizophrenia and bipolar disorder with GWAS: A systematic review.
PMID: 31096178
J Psychiatr Res · 2019
0.60