METTL2A
tRNA N(3)-cytidine methyltransferase METTL2A
Also known as: FLJ12760, MET2A_HUMAN, METTL2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96IZ6
- Gene
- METTL2A
- Ensembl
- ENSG00000087995
- Chromosome
- 17
- Canonical length
- 378 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
OverviewNCBI Gene
Enables tRNA (cytidine-3-)-methyltransferase activity. Involved in tRNA methylation. Located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
378 residues, UniProt reviewed canonical sequence.
>Q96IZ6|METTL2A
1 MAGSYPEGAP AVLADKRQQF GSRFLRDPAR VFHHNAWDNV EWSEEQAAAA ERKVQENSIQ
61 RVCQEKQVDY EINAHKYWND FYKIHENGFF KDRHWLFTEF PELAPSQNQN HLKDWFLENK
121 SEVPECRNNE DGPGLIMEEQ HKCSSKSLEH KTQTLPVEEN VTQKISDLEI CADEFPGSSA
181 TYRILEVGCG VGNTVFPILQ TNNDPGLFVY CCDFSSTAIE LVQTNSEYDP SRCFAFVHDL
241 CDEEKSYPVP KGSLDIIILI FVLSAIVPDK MQKAINRLSR LLKPGGMMLL RDYGRYDMAQ
301 LRFKKGQCLS GNFYVRGDGT RVYFFTQEEL DTLFTTAGLE KVQNLVDRRL QVNRGKQLTM
361 YRVWIQCKYC KPLLSSTSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against METTL2A 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)
- 0.34
- Highest tissue expression
- 5.9 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 5.9 nTPM
- cerebral cortex: 3.7 nTPM
- skin: 3.6 nTPM
- amygdala: 2.9 nTPM
- thyroid gland: 2.9 nTPM
- basal ganglia: 2.8 nTPM
Single-cell type
- erythrocyte progenitors: 45 nCPM
- megakaryocytes: 43 nCPM
- cytotrophoblasts: 32 nCPM
- esophageal basal cells: 32 nCPM
- alveolar cells type 1: 32 nCPM
- late primary spermatocytes: 31 nCPM
Immune cell
- NK-cell: 2.4 nTPM
- neutrophil: 2.2 nTPM
- gdT-cell: 1.9 nTPM
- naive B-cell: 1.8 nTPM
- naive CD8 T-cell: 1.8 nTPM
- basophil: 1.7 nTPM
Brain region
- cerebellum: 8.9 nTPM
- hypothalamus: 8.5 nTPM
- choroid plexus: 8.4 nTPM
- white matter: 8.4 nTPM
- cerebral cortex: 8.2 nTPM
- thalamus: 8.2 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)
- 1.35
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.07
- DepMap mean gene effect
- -0.14
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 9% 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 METTL2A 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 METTL2A as an antibody target. Whether an autoantibody or antibody against METTL2A could matter depends on whether native METTL2A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
METTL2A 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 METTL2A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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