METTL21C
Protein-lysine methyltransferase METTL21C
Also known as: C13orf39, LOC196541, MT21C_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q5VZV1
- Gene
- METTL21C
- Ensembl
- ENSG00000139780
- Chromosome
- 13
- Canonical length
- 264 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
Enables heat shock protein binding activity and protein-lysine N-methyltransferase activity. Involved in peptidyl-lysine methylation. Located in cytoplasm and nucleus. Part of protein-containing complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
264 residues, UniProt reviewed canonical sequence.
>Q5VZV1|METTL21C
1 MDVCLSSAQQ PGRRGEGLSS PGGWLEAEKK GAPQKDSTGG VLEESNKIEP SLHSLQKFVP
61 TDYASYTQEH YRFAGKEIVI QESIESYGAV VWPGAMALCQ YLEEHAEELN FQDAKILEIG
121 AGPGLVSIVA SILGAQVTAT DLPDVLGNLQ YNLLKNTLQC TAHLPEVKEL VWGEDLDKNF
181 PKSAFYYDYV LASDVVYHHY FLDKLLTTMV YLSQPGTVLL WANKFRFSTD YEFLDKFKQV
241 FDTTLLAEYP ESSVKLFKGI LKWDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against METTL21C 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)
- 0.33
- Highest tissue expression
- 23 nTPM
Expression across tissuesHPA
Tissue
- epididymis: 23 nTPM
- skeletal muscle: 4 nTPM
- seminal vesicle: 1.3 nTPM
- placenta: 1 nTPM
- cerebral cortex: 0.8 nTPM
- prostate: 0.6 nTPM
Single-cell type
- epididymal principal cells: 28 nCPM
- late spermatids: 7.8 nCPM
- retinal ganglion cells: 7.7 nCPM
- myonuclei: 6.8 nCPM
- cytotrophoblasts: 4.8 nCPM
- early spermatids: 3.3 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebral cortex: 4.9 nTPM
- cerebellum: 4.6 nTPM
- choroid plexus: 3.2 nTPM
- white matter: 3 nTPM
- hippocampal formation: 2.8 nTPM
- basal ganglia: 2.5 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)
- 1.45
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.08
- 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
- cellular response to dexamethasone stimulus
- hormone-mediated apoptotic signaling pathway
- peptidyl-lysine methylation
- protein methylation
- regulation of release of sequestered calcium ion into cytosol by sarcoplasmic reticulum
- skeletal muscle tissue development
Molecular functions
- heat shock protein binding
- protein methyltransferase activity
- protein-lysine N-methyltransferase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads METTL21C as an antibody target. Whether an autoantibody or antibody against METTL21C could matter depends on whether native METTL21C is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
METTL21C 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 METTL21C as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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