Seroatlas · Human Serome Atlas

CHI3L1

Chitinase-3-like protein 1

Also known as: CH3L1_HUMAN, GP39, YK-40, YKL40

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
P36222
Gene
CHI3L1
Ensembl
ENSG00000133048
Chromosome
1
Canonical length
383 aa
Protein class
Cancer-related genes, Disease related genes, Human disease related genes, Metabolic proteins, Plasma proteins, Predicted intracellular proteins, Predicted secreted proteins
Subcellular location
Golgi apparatus,Vesicles
Secretome location
Secreted to blood

OverviewNCBI Gene

Chitinases catalyze the hydrolysis of chitin, which is an abundant glycopolymer found in insect exoskeletons and fungal cell walls. The glycoside hydrolase 18 family of chitinases includes eight human family members. This gene encodes a glycoprotein member of the glycosyl hydrolase 18 family. The protein lacks chitinase activity and is secreted by activated macrophages, chondrocytes, neutrophils and synovial cells. The protein is thought to play a role in the process of inflammation and tissue remodeling. [provided by RefSeq, Sep 2009]

Canonical amino-acid sequenceUniProt

383 residues, UniProt reviewed canonical sequence.

>P36222|CHI3L1
     1  MGVKASQTGF VVLVLLQCCS AYKLVCYYTS WSQYREGDGS CFPDALDRFL CTHIIYSFAN
    61  ISNDHIDTWE WNDVTLYGML NTLKNRNPNL KTLLSVGGWN FGSQRFSKIA SNTQSRRTFI
   121  KSVPPFLRTH GFDGLDLAWL YPGRRDKQHF TTLIKEMKAE FIKEAQPGKK QLLLSAALSA
   181  GKVTIDSSYD IAKISQHLDF ISIMTYDFHG AWRGTTGHHS PLFRGQEDAS PDRFSNTDYA
   241  VGYMLRLGAP ASKLVMGIPT FGRSFTLASS ETGVGAPISG PGIPGRFTKE AGTLAYYEIC
   301  DFLRGATVHR ILGQQVPYAT KGNQWVGYDD QESVKSKVQY LKDRQLAGAM VWALDLDDFQ
   361  GSFCGQDLRF PLTNAIKDAL AAT

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against CHI3L1 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)
0.24
Highest tissue expression
424 nTPM

Expression across tissuesHPA

Tissue

  • liver: 424 nTPM
  • choroid plexus: 348 nTPM
  • bone marrow: 220 nTPM
  • midbrain: 181 nTPM
  • basal ganglia: 168 nTPM
  • cerebral cortex: 154 nTPM

Single-cell type

  • endometrial secretory cells: 203 nCPM
  • neutrophil progenitors: 161 nCPM
  • podocytes: 153 nCPM
  • breast secretory cells: 128 nCPM
  • alveolar cells type 2: 106 nCPM
  • decidual stromal cells: 96 nCPM

Immune cell

  • neutrophil: 472 nTPM
  • total PBMC: 1.3 nTPM
  • non-classical monocyte: 0.9 nTPM
  • eosinophil: 0.7 nTPM
  • classical monocyte: 0.4 nTPM
  • intermediate monocyte: 0.1 nTPM

Brain region

  • medulla oblongata: 429 nTPM
  • thalamus: 269 nTPM
  • pons: 216 nTPM
  • hypothalamus: 205 nTPM
  • midbrain: 166 nTPM
  • cerebral cortex: 88 nTPM

DiseaseUniProt · ClinVar · IEDB · PubMed

Four sources answering four different questions about CHI3L1.

Disease | AllUniProt

Conditions CHI3L1 is implicated in, by any mechanism.

Disease | ImmuneIEDB

Conditions an epitope on CHI3L1 was assayed in.

ReferencesPubMed · IEDB

Publications for CHI3L1 from three distinct lines of evidence, kept separate because they answer different questions: whether antibodies are directed at the protein, whether a B-cell epitope has been mapped on it, and whether a T-cell epitope has. Each is labelled with its source.

Sources: PubMed — antigen-level antibody evidence from a custom retrieval. Records matching a controlled set of autoantibody terms (the MeSH descriptors Autoantibodies and Autoantigens, with title and abstract term variants) were obtained through NCBI E-utilities, and their titles and abstracts parsed for constructions that direct an antibody at a named protein rather than for co-occurrence. Captured names were resolved against UniProt nomenclature and each antigen adjudicated individually against the source text. IEDB — curated epitope assays from the Immune Epitope Database (Vita et al., Nucleic Acids Research 2019). Bibliographic records from PubMed and MeSH, U.S. National Library of Medicine; citation metrics from NIH iCite (Hutchins et al., PLoS Biology 2016). Titles link to PubMed; abstracts are not reproduced here. The NLM does not endorse this analysis.

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)
0.92
gnomAD pLI
0
gnomAD missense Z
-0.58
DepMap mean gene effect
0.07
DepMap dependency class
none

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% 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

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads CHI3L1 as an antibody target. Whether an autoantibody or antibody against CHI3L1 could matter depends on whether native CHI3L1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

CHI3L1 is annotated as secreted, so native CHI3L1 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 CHI3L1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/CHI3L1. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

Loading the interactive Seroatlas protein explorer...