TRMT61A
tRNA (adenine(58)-N(1))-methyltransferase catalytic subunit TRMT61A
Also known as: C14orf172, FLJ40452, GCD14, Gcd14p, hTRM61, TRM61_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96FX7
- Gene
- TRMT61A
- Ensembl
- ENSG00000166166
- Chromosome
- 14
- Canonical length
- 289 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Mitochondria
OverviewNCBI Gene
Enables mRNA (adenine-N1-)-methyltransferase activity. Involved in mRNA processing. Part of tRNA (m1A) methyltransferase complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
289 residues, UniProt reviewed canonical sequence.
>Q96FX7|TRMT61A
1 MSFVAYEELI KEGDTAILSL GHGAMVAVRV QRGAQTQTRH GVLRHSVDLI GRPFGSKVTC
61 GRGGWVYVLH PTPELWTLNL PHRTQILYST DIALITMMLE LRPGSVVCES GTGSGSVSHA
121 IIRTIAPTGH LHTVEFHQQR AEKAREEFQE HRVGRWVTVR TQDVCRSGFG VSHVADAVFL
181 DIPSPWEAVG HAWDALKVEG GRFCSFSPCI EQVQRTCQAL AARGFSELST LEVLPQVYNV
241 RTVSLPPPDL GTGTDGPAGS DTSPFRSGTP MKEAVGHTGY LTFATKTPGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TRMT61A 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)
- 0.28
- Highest tissue expression
- 24 nTPM
Expression across tissuesHPA
Tissue
- colon: 24 nTPM
- urinary bladder: 19 nTPM
- basal ganglia: 18 nTPM
- endometrium: 18 nTPM
- fallopian tube: 18 nTPM
- prostate: 17 nTPM
Single-cell type
- decidual stromal cells: 35 nCPM
- esophageal basal cells: 31 nCPM
- alveolar cells type 1: 24 nCPM
- late spermatids: 24 nCPM
- suprabasal keratinocytes: 23 nCPM
- basal keratinocytes: 23 nCPM
Immune cell
- non-classical monocyte: 11 nTPM
- intermediate monocyte: 5.4 nTPM
- myeloid DC: 3.3 nTPM
- memory CD8 T-cell: 2.8 nTPM
- NK-cell: 2.7 nTPM
- gdT-cell: 2.6 nTPM
Brain region
- basal ganglia: 21 nTPM
- white matter: 19 nTPM
- cerebral cortex: 18 nTPM
- medulla oblongata: 18 nTPM
- thalamus: 17 nTPM
- midbrain: 17 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about TRMT61A.
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 47 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
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)
- 0.97
- gnomAD pLI
- 0.02
- gnomAD missense Z
- 1.28
- DepMap mean gene effect
- -0.18
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% 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 TRMT61A 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 TRMT61A as an antibody target. Whether an autoantibody or antibody against TRMT61A could matter depends on whether native TRMT61A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TRMT61A 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 TRMT61A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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