1 sources retrieved Β· Most recent: April 2026 Β· Index updated 15 days ago
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20PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITYβ Experimental GO Evidenceβ Swiss-Prot Reviewed
tRNA methylationtRNA (uridine) methyltransferase activitymethyltransferase activitycytoplasmneurodegenerative diseaselymphatic system diseasevein disorderPathologic fracture
Based on limited published evidence, TRMT44 encodes a probable adenosyl-L-methionine (AdoMet)-dependent tRNA methyltransferase with tRNA (uridine) methyltransferase activity. The protein catalyzes methylation of uracil residues in transfer RNA molecules, a post-transcriptional modification essential for tRNA function. TRMT44 was identified as a hub gene in co-expression network analysis associated with recurrent early pregnancy loss, suggesting potential involvement in reproductive processes 1, though the mechanistic connection to pregnancy loss remains unclear.
1
TRMT44 identified as a hub gene in MEbrown module associated with recurrent early pregnancy loss and enriched in cell adhesion and TGF-Ξ² signaling pathway functions
PMID: 32401299β Limited data available β This gene has 1 indexed publication. Summary and analysis may be incomplete.
neurodegenerative diseaseOpen Targets
lymphatic system diseaseOpen Targets
vein disorderOpen Targets
Pathologic fractureOpen Targets
Abruptio PlacentaeOpen Targets
mouth diseaseOpen Targets
Abnormality of the skeletal systemOpen Targets
atrial fibrillationOpen Targets
carpal tunnel syndromeOpen Targets
systemic lupus erythematosusOpen Targets
osteoarthritis, hipOpen Targets
subarachnoid hemorrhageOpen Targets
mononeuropathyOpen Targets
No pathogenic variants reported on ClinVar for this gene.