LCN2
Neutrophil gelatinase-associated lipocalin
Also known as: 24p3, NGAL, NGAL_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P80188
- Gene
- LCN2
- Ensembl
- ENSG00000148346
- Chromosome
- 9
- Canonical length
- 198 aa
- Protein class
- Candidate cardiovascular disease genes, Plasma proteins, Predicted secreted proteins
- Subcellular location
- Endoplasmic reticulum
- Secretome location
- Secreted in other tissues
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a protein that belongs to the lipocalin family. Members of this family transport small hydrophobic molecules such as lipids, steroid hormones and retinoids. The protein encoded by this gene is a neutrophil gelatinase-associated lipocalin and plays a role in innate immunity by limiting bacterial growth as a result of sequestering iron-containing siderophores. The presence of this protein in blood and urine is an early biomarker of acute kidney injury. This protein is thought to be be involved in multiple cellular processes, including maintenance of skin homeostasis, and suppression of invasiveness and metastasis. Mice lacking this gene are more susceptible to bacterial infection than wild type mice. [provided by RefSeq, Sep 2015]
Canonical amino-acid sequenceUniProt
198 residues, UniProt reviewed canonical sequence.
>P80188|LCN2
1 MPLGLLWLGL ALLGALHAQA QDSTSDLIPA PPLSKVPLQQ NFQDNQFQGK WYVVGLAGNA
61 ILREDKDPQK MYATIYELKE DKSYNVTSVL FRKKKCDYWI RTFVPGCQPG EFTLGNIKSY
121 PGLTSYLVRV VSTNYNQHAM VFFKKVSQNR EYFKITLYGR TKELTSELKE NFIRFSKSLG
181 LPENHIVFPV PIDQCIDGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LCN2 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.32
- Highest tissue expression
- 2,617 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 2,617 nTPM
- gallbladder: 2,091 nTPM
- salivary gland: 1,266 nTPM
- cervix: 764 nTPM
- esophagus: 644 nTPM
- urinary bladder: 627 nTPM
Single-cell type
- endometrial secretory cells: 17,173 nCPM
- esophageal apical cells: 9,320 nCPM
- conjunctival goblet cells: 8,400 nCPM
- prostatic club cells: 6,845 nCPM
- salivary duct cells: 4,478 nCPM
- lacrimal acinar cells: 3,931 nCPM
Immune cell
- total PBMC: 12 nTPM
- neutrophil: 12 nTPM
- basophil: 9.7 nTPM
- non-classical monocyte: 4.7 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
Brain region
- choroid plexus: 4.2 nTPM
- medulla oblongata: 0.7 nTPM
- pons: 0.7 nTPM
- cerebral cortex: 0.6 nTPM
- basal ganglia: 0.4 nTPM
- cerebellum: 0.4 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about LCN2.
Disease | ImmuneIEDB
Conditions an epitope on LCN2 was assayed in.
- invasive ductal carcinoma T cell
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.72
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.43
- DepMap mean gene effect
- -0.12
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- acute-phase response
- cellular response to amyloid-beta
- cellular response to hydrogen peroxide
- cellular response to hypoxia
- cellular response to increased oxygen levels
- cellular response to interleukin-1
- cellular response to interleukin-6
- cellular response to lipopolysaccharide
- cellular response to nerve growth factor stimulus
- cellular response to nutrient levels
- cellular response to tumor necrosis factor
- cellular response to X-ray
- defense response to bacterium
- extrinsic apoptotic signaling pathway in absence of ligand
- innate immune response
- long-term memory
- negative regulation of hippocampal neuron apoptotic process
- positive regulation of cell projection organization
- positive regulation of cold-induced thermogenesis
- positive regulation of endothelial cell migration
- positive regulation of endothelial tube morphogenesis
- positive regulation of gene expression
- positive regulation of iron ion import across plasma membrane
- positive regulation of reactive oxygen species biosynthetic process
- response to blue light
- response to fructose
- response to herbicide
- response to iron(II) ion
- response to kainic acid
- response to mycotoxin
- response to virus
- response to xenobiotic stimulus
- short-term memory
- siderophore transport
- positive regulation of hippocampal neuron apoptotic process
Molecular functions
- enterobactin binding
- identical protein binding
- iron ion binding
- iron ion sequestering activity
- protease binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Lipocalin/cytosolic fatty-acid binding domain
- Lipocalin
- Calycin
- Lipocalin family conserved site
- Lipocalin / cytosolic fatty-acid binding protein family
- Neutrophil gelatinase-associated lipocalin/epididymal-specific lipocalin-12
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of LCN2 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads LCN2 as an antibody target. Whether an autoantibody or antibody against LCN2 could matter depends on whether native LCN2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LCN2 is annotated as secreted, so native LCN2 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label LCN2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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