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10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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LXN
latexin
Chromosome 3 · 3q25.32
NCBI Gene: 56925Ensembl: ENSG00000079257.8HGNC: HGNC:13347UniProt: Q9BS40
26PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
protein bindingmetalloendopeptidase inhibitor activityGO:0005615cytoplasmhepatoencephalopathy due to combined oxidative phosphorylation defect type 1combined oxidative phosphorylation deficiencyLeigh syndromeheart failure
✦AI Summary

LXN (latexin) is a metallocarboxypeptidase inhibitor that functions as a key regulator of cellular homeostasis and inflammatory responses across multiple organ systems. The protein acts as a hardly reversible, non-competitive inhibitor of carboxypeptidases CPA1, CPA2, and CPA4, and plays critical roles in inflammation regulation 1. LXN negatively regulates hematopoietic stem cell (HSC) population size by enhancing apoptosis and decreasing self-renewal through interaction with ribosomal protein subunit 3 (Rps3) 2. In vascular biology, LXN regulates endothelial cell cytoskeletal remodeling by controlling Filamin A proteolytic cleavage and nuclear translocation, with LXN deficiency improving vascular permeability and protecting against atherosclerosis 34. The protein also functions as an inflammatory suppressor in colitis through the HECTD1/Rps3/NF-κB pathway, where LXN deficiency leads to enhanced inflammatory responses 1. Additionally, LXN has been implicated in renal epithelial cell senescence and macrophage polarization in nephrolithiasis 5. LXN expression is altered in various pathological conditions including colorectal cancer, sarcopenia, and type 2 diabetes mellitus, suggesting its broad physiological significance 67.

Sources cited
1
LXN negatively regulates HSC population size by enhancing apoptosis and decreasing self-renewal through interaction with Rps3
PMID: 29608488
2
LXN functions as an inflammatory suppressor and regulates colitis through HECTD1/Rps3/NF-κB pathway
PMID: 32555320
3
LXN regulates endothelial cell cytoskeletal remodeling by controlling Filamin A proteolytic cleavage
PMID: 34085389
4
LXN deficiency protects against atherosclerosis by promoting anti-inflammatory macrophage phenotype
PMID: 39424784
5
LXN is involved in renal epithelial cell senescence and macrophage polarization in nephrolithiasis
PMID: 41112268
6
LXN expression is altered in colorectal cancer tumor heterogeneity
PMID: 38729966
7
LXN is identified as a shared gene between sarcopenia and type 2 diabetes mellitus
PMID: 35271662
Disease Associationsⓘ20
hepatoencephalopathy due to combined oxidative phosphorylation defect type 1Open Targets
0.57Moderate
combined oxidative phosphorylation deficiencyOpen Targets
0.34Weak
Leigh syndromeOpen Targets
0.27Weak
heart failureOpen Targets
0.24Weak
genetic disorderOpen Targets
0.19Weak
Developmental regressionOpen Targets
0.12Weak
Relative macrocephalyOpen Targets
0.12Weak
Severe muscular hypotoniaOpen Targets
0.12Weak
neoplasmOpen Targets
0.11Weak
melanomaOpen Targets
0.08Suggestive
hypertensionOpen Targets
0.08Suggestive
atherosclerosisOpen Targets
0.08Suggestive
obesityOpen Targets
0.07Suggestive
colitisOpen Targets
0.07Suggestive
gastric cancerOpen Targets
0.05Suggestive
cancerOpen Targets
0.04Suggestive
lymphomaOpen Targets
0.04Suggestive
pathological myopiaOpen Targets
0.04Suggestive
Abruptio PlacentaeOpen Targets
0.04Suggestive
ovarian carcinomaOpen Targets
0.04Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar ↗
Related Genes
CPA4Protein interaction100%CPA2Protein interaction81%
Tissue Expression6 tissues
Bone Marrow
100%
Ovary
89%
Lung
54%
Heart
20%
Brain
7%
Liver
7%
Gene Interaction Network
Click a node to explore
LXNCPA4CPA2
PROTEIN STRUCTURE
Preparing viewer…
PDB2BO9 · 1.60 Å · X-ray
View on RCSB ↗
Constraintⓘ
LOEUFⓘ
1.27LoF Tolerant
pLIⓘ
0.00Tolerant
Observed/Expected LoF0.93 [0.70–1.27]
RankingsWhere LXN stands among ~20K protein-coding genes
  • #12,818of 20,598
    Most Researched26
  • #13,372of 17,882
    Most Constrained (LOEUF)1.27
Genes detectedLXN
Sources retrieved10 papers
Response time—
📄 Sources
10▼
1
Integrating spatial and single-cell transcriptomics reveals tumor heterogeneity and intercellular networks in colorectal cancer.
PMID: 38729966
Cell Death Dis · 2024
1.00
2
Identification of the shared gene signatures and pathways between sarcopenia and type 2 diabetes mellitus.
PMID: 35271662
PLoS One · 2022
0.90
3
Latexin deficiency limits foam cell formation and ameliorates atherosclerosis by promoting macrophage phenotype differentiation.
PMID: 39424784
Cell Death Dis · 2024
0.80
4
Latexin and hematopoiesis.
PMID: 29608488
Curr Opin Hematol · 2018
0.70
5
HIF-1α-HPRT1 axis promotes tumorigenesis and gefitinib resistance by enhancing purine metabolism in EGFR-mutant lung adenocarcinoma.
PMID: 39343971
J Exp Clin Cancer Res · 2024
0.60