Gene Gene information from NCBI Gene database.
Entrez ID 115708
Gene name TRNA methyltransferase 61A
Gene symbol TRMT61A
Synonyms (NCBI Gene)
C14orf172GCD14Gcd14pTRM61hTRM61
Chromosome 14
Chromosome location 14q32.33
miRNA miRNA information provided by mirtarbase database.
189
miRTarBase ID miRNA Experiments Reference
MIRT049081 hsa-miR-92a-3p CLASH 23622248
MIRT043665 hsa-miR-342-3p CLASH 23622248
MIRT039179 hsa-miR-769-5p CLASH 23622248
MIRT1456920 hsa-miR-1185 CLIP-seq
MIRT1456921 hsa-miR-1207-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
18
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 16043508, 28514442, 32296183, 33961781
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IEA
GO:0005634 Component Nucleus NAS 16043508
GO:0005654 Component Nucleoplasm TAS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620885 23790 ENSG00000166166
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96FX7
Protein name tRNA (adenine(58)-N(1))-methyltransferase catalytic subunit TRMT61A (EC 2.1.1.220) (mRNA methyladenosine-N(1)-methyltransferase catalytic subunit TRMT61A) (EC 2.1.1.-) (tRNA(m1A58)-methyltransferase subunit TRMT61A) (tRNA(m1A58)MTase subunit TRMT61A)
Protein function Catalytic subunit of tRNA (adenine-N(1)-)-methyltransferase, which catalyzes the formation of N(1)-methyladenine at position 58 (m1A58) in initiator methionyl-tRNA (PubMed:16043508). Catalytic subunit of mRNA N(1)-methyltransferase complex, whic
PDB 5CCB , 5CCX , 5CD1
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF08704 GCD14 64 286 tRNA methyltransferase complex GCD14 subunit Family
Sequence
Sequence length 289
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    tRNA modification in the nucleus and cytosol
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
10
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ATTENTION DEFICIT HYPERACTIVITY DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AUTISM SPECTRUM DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BASAL CELL CARCINOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BONE FRACTURE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Carcinoma Hepatocellular Associate 37170222
★☆☆☆☆
Found in Text Mining only
De Lange Syndrome Associate 40361155
★☆☆☆☆
Found in Text Mining only
Depressive Disorder Major Associate 36672180
★☆☆☆☆
Found in Text Mining only
Hearing Loss Associate 40361155
★☆☆☆☆
Found in Text Mining only
Hepatoblastoma Associate 37850543
★☆☆☆☆
Found in Text Mining only
Urinary Bladder Neoplasms Associate 35444240
★☆☆☆☆
Found in Text Mining only