LECT2
Leukocyte cell-derived chemotaxin-2
Also known as: chm-II, chm2, LECT2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O14960
- Gene
- LECT2
- Ensembl
- ENSG00000145826
- Chromosome
- 5
- Canonical length
- 151 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins, Predicted secreted proteins
- Subcellular location
- Vesicles,Cytosol
- Secretome location
- Secreted to blood
OverviewNCBI Gene
This gene encodes a secreted, 16 kDa protein that acts as a chemotactic factor to neutrophils and stimulates the growth of chondrocytes and osteoblasts. This protein has high sequence similarity to the chondromodulin repeat regions of the chicken myb-induced myeloid 1 protein. A polymorphism in this gene may be associated with rheumatoid arthritis. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
151 residues, UniProt reviewed canonical sequence.
>O14960|LECT2
1 MFSTKALLLA GLISTALAGP WANICAGKSS NEIRTCDRHG CGQYSAQRSQ RPHQGVDILC
61 SAGSTVYAPF TGMIVGQEKP YQNKNAINNG VRISGRGFCV KMFYIKPIKY KGPIKKGEKL
121 GTLLPLQKVY PGIQSHVHIE NCDSSDPTAY LLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LECT2 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)
- 0.33
- Highest tissue expression
- 445 nTPM
Expression across tissuesHPA
Tissue
- liver: 445 nTPM
- testis: 8.3 nTPM
- retina: 2.3 nTPM
- bone marrow: 2 nTPM
- skeletal muscle: 1.9 nTPM
- skin: 1.1 nTPM
Single-cell type
- early spermatids: 152 nCPM
- hepatocytes: 107 nCPM
- late primary spermatocytes: 104 nCPM
- late spermatids: 64 nCPM
- retinal horizontal cells: 28 nCPM
- retinal ganglion cells: 12 nCPM
Immune cell
- basophil: 0.6 nTPM
- memory B-cell: 0.2 nTPM
- eosinophil: 0.1 nTPM
- memory CD4 T-cell: 0.1 nTPM
- memory CD8 T-cell: 0.1 nTPM
- naive B-cell: 0.1 nTPM
Brain region
- cerebellum: 27 nTPM
- cerebral cortex: 20 nTPM
- white matter: 17 nTPM
- basal ganglia: 17 nTPM
- hypothalamus: 16 nTPM
- amygdala: 15 nTPM
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)
- 1.45
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.09
- DepMap mean gene effect
- 0.17
- DepMap dependency class
- none
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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Leukocyte cell-derived chemotaxin 2
- Duplicated hybrid motif
- M23ase, beta-sheet core domain
- Leukocyte cell-derived chemotaxin 2, chordata
- Peptidase family M23
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of LECT2 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 LECT2 as an antibody target. Whether an autoantibody or antibody against LECT2 could matter depends on whether native LECT2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LECT2 is annotated as secreted, so native LECT2 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 LECT2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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