1. Gene
  2. TRMO - tRNA methyltransferase O Gene

TRMO - tRNA methyltransferase O Gene

Homo sapiens

Also known as NAP1; HSPC219; C9orf156

Gene ID: 51531 | Gene type: protein coding

About TRMO

This gene has 6 transcripts (splice variants) and 173 orthologues. Ubiquitous expression in thyroid (RPKM 2.2), lymph node (RPKM 1.5) and 25 other tissues.

Summary

Enables tRNA (adenine-N6-)-methyltransferase activity. Involved in tRNA methylation. [provided by Alliance of Genome Resources, Apr 2022]

TRMO Products(7)

mRNA Protein Name
NM_001330725.2 NP_001317654.1 tRNA (adenine(37)-N6)-methyltransferase isoform 2
NM_001371657.1 NP_001358586.1 tRNA (adenine(37)-N6)-methyltransferase isoform 1
NM_001371658.1 NP_001358587.1 tRNA (adenine(37)-N6)-methyltransferase isoform 3
NM_001371659.1 NP_001358588.1 tRNA (adenine(37)-N6)-methyltransferase isoform 4
NM_001371660.1 NP_001358589.1 tRNA (adenine(37)-N6)-methyltransferase isoform 2
NM_001371661.1 NP_001358590.1 tRNA (adenine(37)-N6)-methyltransferase isoform 2
NM_016481.5 NP_057565.3 tRNA (adenine(37)-N6)-methyltransferase isoform 1
Gene Ontology
  • Molecular Function
  • Biological Process
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
enables tRNA (L-threonylcarbamoyladenosine(37)-C2) methyltransferase activity IDA
IDA: Inferred from direct assay
25063302 GOA
Biological Process GO Annotation Evidence Reference Source
involved in tRNA methylation IDA
IDA: Inferred from direct assay
25063302 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

TRMO Protein Structure

UPF0066

UPF0066: Uncharacterised protein family UPF0066 (43 - 164)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 441 a.a.
Protein Preferred Names Protein Names

tRNA (adenine(37)-N6)-methyltransferase

Nef (lentivirus myristoylated factor) associated protein 1

TRMO Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
TRMO Q9BU70 SPATC1L Homo sapiens Q9H0A9-2 32296183
Intra
TRMO Q9BU70 SPATC1L Homo sapiens Q9H0A9-2 32296183
Intra
TRMO Q9BU70 SPATC1L Homo sapiens Q9H0A9-2 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Arthrogryposis, Distal, Type 6

Distal Arthrogryposis Type 6

DA6

Arthrogryposis-Like Hand Anomaly-Sensorineural Deafness Syndrome

Arthrogryposis And Sensorineural Deafness

Familial Hand Abnormality And Sensori-Neural Deafness

Arthrogryposis-Like Hand Anomaly And Sensorineural Deafness

Arthrogryposis-Like Hand Anomaly-Sensorineural Hearing Loss Syndrome

Thiamine-Responsive Megaloblastic Anemia Syndrome

TRMA

Rogers Syndrome

Thiamine-Responsive Myelodysplasia

Thiamine-Responsive Anemia Syndrome

Thiamine Metabolism Dysfunction Syndrome 1

Thmd1

Megaloblastic Anemia, Thiamine-Responsive, With Diabetes Mellitus And Sensorineural Deafness

Thiamine-Responsive Megaloblastic Anemia With Diabetes Mellitus And Sensorineural Deafness

Thiamine Responsive Megaloblastic Anemia Syndrome

Megaloblastic Anemia Thiamine-Responsive With Diabetes Mellitus And Sensorineural Deafness

Thiamine-Responsive Megaloblastic Anemia

Thiamine-Responsive Anaemia Syndrome

Thiamine-Responsive Megaloblastic Anaemia Syndrome

Thiamine-Responsive Megaloblastic Anaemia With Diabetes Mellitus And Sensorineural Deafness

Thiamine-Responsive Megaloblastic Anemia With Diabetes Mellitus And Sensorineural Hearing Loss

Cleft Palate, Isolated

Cleft Palate

Isolated Cleft Palate

CPI

Cp

Palatoschisis

Cleft Palate Isolated

Uranostaphyloschisis

Congenital Fissure Of Palate

Cleft Of Secondary Palate

Galloway-Mowat Syndrome

Galloway Mowat Syndrome

Galloway Syndrome

Hiatal Hernia-Microcephaly-Nephrosis, Galloway Type

Microcephaly Nephrosis Syndrome

Microcephaly, Hiatal Hernia, And Nephrotic Syndrome

Nephrosis Neuronal Dysmigration Syndrome

Microcephaly-Hiatus Hernia-Nephrotic Syndrome

Nephrosis-Neuronal Dysmigration Syndrome

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Macaca mulatta TRMO VGNC VGNC:79907
Mus musculus TRMO MGD MGI:1922003
Bos taurus TRMO VGNC VGNC:36364
Rattus norvegicus TRMO RGD RGD:1305420
Felis catus TRMO VGNC VGNC:66564
Canis familiaris TRMO VGNC VGNC:47849