METTL2B
tRNA N(3)-cytidine methyltransferase METTL2B
Also known as: FLJ11350, MET2B_HUMAN, METL, METTL2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6P1Q9
- Gene
- METTL2B
- Ensembl
- ENSG00000165055
- Chromosome
- 7
- Canonical length
- 378 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins
OverviewNCBI Gene
This gene is a member of a family of methyltransferases that share homology with, but are distinct from, the UbiE family of methyltransferases. Alternatively spliced variants which encode different protein isoforms have been described; however, not all variants have been fully characterized. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
378 residues, UniProt reviewed canonical sequence.
>Q6P1Q9|METTL2B
1 MAGSYPEGAP AILADKRQQF GSRFLSDPAR VFHHNAWDNV EWSEEQAAAA ERKVQENSIQ
61 RVCQEKQVDY EINAHKYWND FYKIHENGFF KDRHWLFTEF PELAPSQNQN HLKDWFLENK
121 SEVCECRNNE DGPGLIMEEQ HKCSSKSLEH KTQTPPVEEN VTQKISDLEI CADEFPGSSA
181 TYRILEVGCG VGNTVFPILQ TNNDPGLFVY CCDFSSTAIE LVQTNSEYDP SRCFAFVHDL
241 CDEEKSYPVP KGSLDIIILI FVLSAVVPDK MQKAINRLSR LLKPGGMVLL RDYGRYDMAQ
301 LRFKKGQCLS GNFYVRGDGT RVYFFTQEEL DTLFTTAGLE KVQNLVDRRL QVNRGKQLTM
361 YRVWIQCKYC KPLLSSTSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against METTL2B 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)
- 0.35
- Highest tissue expression
- 7.7 nTPM
Expression across tissuesHPA
Tissue
- liver: 7.7 nTPM
- skin: 7.4 nTPM
- skeletal muscle: 6.5 nTPM
- cerebral cortex: 5.8 nTPM
- retina: 5.8 nTPM
- hypothalamus: 5.7 nTPM
Single-cell type
- choroid plexus epithelial cells: 43 nCPM
- podocytes: 40 nCPM
- renal collecting duct intercalated cells: 39 nCPM
- distal convoluted tubule cells: 35 nCPM
- adipocytes: 34 nCPM
- renal connecting tubule cells: 34 nCPM
Immune cell
- basophil: 2.7 nTPM
- naive CD8 T-cell: 2.4 nTPM
- gdT-cell: 2.1 nTPM
- naive B-cell: 2.1 nTPM
- memory CD4 T-cell: 1.9 nTPM
- naive CD4 T-cell: 1.9 nTPM
Brain region
- cerebellum: 22 nTPM
- white matter: 21 nTPM
- hypothalamus: 19 nTPM
- thalamus: 19 nTPM
- cerebral cortex: 18 nTPM
- basal ganglia: 18 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)
- 1.18
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.1
- DepMap mean gene effect
- -0.11
- 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
- tRNA (cytidine-3-)-methyltransferase activity
- tRNA (cytidine) methyltransferase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of METTL2B 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 METTL2B as an antibody target. Whether an autoantibody or antibody against METTL2B could matter depends on whether native METTL2B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
METTL2B 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 METTL2B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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