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TRMT61A

Gene

tRNA methyltransferase 61A

HGNCHGNC:23790EnsemblENSG00000166166NCBI Gene115708
Locus: gene with protein productLocation: 14q32.33

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asC14orf172 · FLJ40452 · GCD14 · Gcd14p · hTRM61
View full nomenclature history (7)
Previous symbolsC14orf172
Alias symbolsFLJ40452, GCD14, Gcd14p, hTRM61
Previous nameschromosome 14 open reading frame 172, tRNA methyltransferase 61 homolog A (S. cerevisiae)

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Neurodegenerative Diseases
Intelligence
Mental Disorders
De Lange Syndrome
Major depressive disorder
Schizophrenia
Diabetes Mellitus, Type 2
Heart Arrest
Epilepsies, Partial

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

7BS N1-adenosine RNA methyltransferasesDNA/RNA methyltransferases

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.