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GeneE
1 sources retrieved Β· Most recent: April 2026 Β· Index updated 15 days ago
β“˜GeneE is for informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment.
TRMT44
tRNA methyltransferase 44 homolog
Chromosome 4 Β· 4p16.1
NCBI Gene: 152992Ensembl: ENSG00000155275.20HGNC: HGNC:26653UniProt: Q8IYL2
20PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY
βœ“ Experimental GO Evidenceβœ“ Swiss-Prot Reviewed
tRNA methylationtRNA (uridine) methyltransferase activitymethyltransferase activitycytoplasmneurodegenerative diseaselymphatic system diseasevein disorderPathologic fracture
✦AI Summary

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.

Sources cited
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: 32401299
⚠Limited data available β€” This gene has 1 indexed publication. Summary and analysis may be incomplete.
Disease Associationsβ“˜20
neurodegenerative diseaseOpen Targets
0.27Weak
lymphatic system diseaseOpen Targets
0.21Weak
vein disorderOpen Targets
0.19Weak
Pathologic fractureOpen Targets
0.09Suggestive
asphyxiaOpen Targets
0.07Suggestive
HypoxemiaOpen Targets
0.07Suggestive
Abruptio PlacentaeOpen Targets
0.06Suggestive
poisoningOpen Targets
0.06Suggestive
mouth diseaseOpen Targets
0.05Suggestive
skin woundOpen Targets
0.05Suggestive
hemorrhoidOpen Targets
0.05Suggestive
Abnormality of the skeletal systemOpen Targets
0.04Suggestive
amputationOpen Targets
0.04Suggestive
drug allergyOpen Targets
0.04Suggestive
atrial fibrillationOpen Targets
0.03Suggestive
carpal tunnel syndromeOpen Targets
0.03Suggestive
systemic lupus erythematosusOpen Targets
0.02Suggestive
osteoarthritis, hipOpen Targets
0.02Suggestive
subarachnoid hemorrhageOpen Targets
0.02Suggestive
mononeuropathyOpen Targets
0.02Suggestive
Pathogenic Variants
No pathogenic variants reported on ClinVar for this gene.
View on ClinVar β†—
Related Genes
THUMPD3Shared pathway100%TRMOShared pathway100%TRMT5Shared pathway100%TRMT10AShared pathway100%METTL1Protein interaction59%TARBP1Shared pathway50%
Tissue Expression6 tissues
Ovary
100%
Bone Marrow
55%
Liver
37%
Lung
35%
Heart
26%
Brain
15%
Gene Interaction Network
Click a node to explore
TRMT44THUMPD3TRMOTRMT5TRMT10AMETTL1TARBP1
PROTEIN STRUCTURE
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AlphaFoldAI-predicted Β· UniProt Q8IYL2
View on AlphaFold β†—
Constraintβ“˜
LOEUFβ“˜
1.19LoF Tolerant
pLIβ“˜
0.00Tolerant
Observed/Expected LoF0.97 [0.79–1.19]
RankingsWhere TRMT44 stands among ~20K protein-coding genes
  • #14,304of 20,598
    Most Researched20
  • #12,513of 17,882
    Most Constrained (LOEUF)1.19
Genes detectedTRMT44
Sources retrieved1 papers
Response timeβ€”
πŸ“„ Sources
1
1
Weighted gene correlation network analysis reveals novel regulatory modules associated with recurrent early pregnancy loss.
PMID: 32401299
Biosci Rep Β· 2020
1.00