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 DRPCNPLLocalizationUniProt · 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
- aggrephagy
- autophagosome assembly
- autophagosome maturation
- cellular response to nitrogen starvation
- cellular response to starvation
- macroautophagy
- mitophagy
- protein exit from endoplasmic reticulum
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Autophagy protein Atg8 ubiquitin-like
- Ubiquitin-like domain superfamily
- Autophagy protein Atg8 ubiquitin like
- Microtubule-associated protein 1A/1B light chain 3C
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.
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