Seroatlas · Human Serome Atlas

CLEC2L

C-type lectin domain family 2 member L

Also known as: CLC2L_HUMAN, FLJ32986

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

Protein identityUniProt · HPA

UniProt accession
P0C7M8
Gene
CLEC2L
Ensembl
ENSG00000236279
Chromosome
7
Canonical length
214 aa
Protein class
Predicted intracellular proteins, Predicted membrane proteins

OverviewNCBI Gene

Predicted to enable carbohydrate binding activity. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

214 residues, UniProt reviewed canonical sequence.

>P0C7M8|CLEC2L
     1  MEPAREPPSR ARPPPPLAAR PAPAPAAPRP RSPAEAEARG PEGLLRRSGS GYEGSTSWKA
    61  ALEDTTTRLL LGAIAVLLFA ILVVMSILAS KGCIKCEAPC PEDWLLYGRK CYFFSEEPRD
   121  WNTGRQYCHT HEAVLAVIQS QKELEFMFKF TRREPWIGLR RVGDEFHWVN GDPFDPDTFT
   181  IAGPGECVFV EPTRLVSTEC LMTRPWVCSK MAYT

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against CLEC2L 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
Unknown
Secreted
No
Transmembrane segments
1
Mean surface accessibility (rSASA)
0.46
Highest tissue expression
38 nTPM

Expression across tissuesHPA

Tissue

  • cerebral cortex: 38 nTPM
  • cerebellum: 20 nTPM
  • hippocampal formation: 20 nTPM
  • midbrain: 18 nTPM
  • amygdala: 14 nTPM
  • parathyroid gland: 13 nTPM

Single-cell type

  • retinal ganglion cells: 147 nCPM
  • platelets: 65 nCPM
  • other brain neurons: 55 nCPM
  • brain inhibitory neurons: 55 nCPM
  • brain excitatory neurons: 47 nCPM
  • retinal amacrine cells: 35 nCPM

Immune cell

  • total PBMC: 0.1 nTPM
  • basophil: 0 nTPM
  • classical monocyte: 0 nTPM
  • eosinophil: 0 nTPM
  • gdT-cell: 0 nTPM
  • intermediate monocyte: 0 nTPM

Brain region

  • pons: 73 nTPM
  • cerebral cortex: 71 nTPM
  • thalamus: 63 nTPM
  • cerebellum: 56 nTPM
  • medulla oblongata: 53 nTPM
  • white matter: 35 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)
1.12
gnomAD pLI
0.01
gnomAD missense Z
0.53
DepMap mean gene effect
0.01
DepMap dependency class
none

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).

OntologyGO

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads CLEC2L as an antibody target. Whether an autoantibody or antibody against CLEC2L could matter depends on whether native CLEC2L is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

CLEC2L is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.

Annotation status

The present source text does not explicitly label CLEC2L as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/CLEC2L. 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).

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