Seroatlas · Human Serome Atlas

MAP1LC3C

Microtubule-associated protein 1 light chain 3 gamma

Also known as: ATG8J, MLP3C_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
Q9BXW4
Gene
MAP1LC3C
Ensembl
ENSG00000197769
Chromosome
1
Canonical length
147 aa
Protein class
Predicted intracellular proteins
Subcellular location
Cytoplasmic bodies

OverviewNCBI Gene

Autophagy is a highly regulated bulk degradation process that plays an important role in cellular maintenance and development. MAP1LC3C is an ortholog of the yeast autophagosome protein Atg8 (He et al., 2003 [PubMed 12740394]).[supplied by OMIM, Nov 2010]

Canonical amino-acid sequenceUniProt

147 residues, UniProt reviewed canonical sequence.

>Q9BXW4|MAP1LC3C
     1  MPPPQKIPSV RPFKQRKSLA IRQEEVAGIR AKFPNKIPVV VERYPRETFL PPLDKTKFLV
    61  PQELTMTQFL SIIRSRMVLR ATEAFYLLVN NKSLVSMSAT MAEIYRDYKD EDGFVYMTYA
   121  SQETFGCLES AAPRDGSSLE DRPCNPL

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against MAP1LC3C 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
Intracellular
Secreted
No
Transmembrane segments
0
Mean surface accessibility (rSASA)
0.38
Highest tissue expression
13 nTPM

Expression across tissuesHPA

Tissue

  • breast: 13 nTPM
  • adipose tissue: 13 nTPM
  • placenta: 10 nTPM
  • salivary gland: 6.9 nTPM
  • lung: 5.6 nTPM
  • skin: 5.4 nTPM

Single-cell type

  • fibroblasts: 3.7 nCPM
  • kupffer cells: 3.1 nCPM
  • fibro-adipogenic progenitors: 2 nCPM
  • early primary spermatocytes: 1.6 nCPM
  • ovarian stromal cells: 1.4 nCPM
  • adipocytes: 1.2 nCPM

Immune cell

  • non-classical monocyte: 0.6 nTPM
  • basophil: 0.3 nTPM
  • intermediate monocyte: 0.2 nTPM
  • classical monocyte: 0.1 nTPM
  • memory B-cell: 0.1 nTPM
  • naive B-cell: 0.1 nTPM

Brain region

  • cerebral cortex: 4 nTPM
  • choroid plexus: 1.8 nTPM
  • hypothalamus: 1.7 nTPM
  • pons: 1.6 nTPM
  • basal ganglia: 1.5 nTPM
  • white matter: 1.5 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)
1.91
gnomAD pLI
0
gnomAD missense Z
0.5
DepMap mean gene effect
-0.04
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

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

InteractionsUniProt · HPA

Protein binding partners of MAP1LC3C 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 MAP1LC3C as an antibody target. Whether an autoantibody or antibody against MAP1LC3C could matter depends on whether native MAP1LC3C is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

MAP1LC3C 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 MAP1LC3C as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/MAP1LC3C. 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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