TRT-AGT7-1
gene geneOn this page
Also known as tRNA-Thr-AGT-7-1
Summary
TRT-AGT7-1 (tRNA-Thr (AGT) 7-1, HGNC:12352) is a gene on chromosome 17q24.1.
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:12352 |
| Approved symbol | TRT-AGT7-1 |
| Name | tRNA-Thr (AGT) 7-1 |
| Location | 17q24.1 |
| Locus type | RNA, transfer |
| Status | Approved |
| Aliases | tRNA-Thr-AGT-7-1 |
| Entrez | 7238 |
| RNAcentral | URS00006E1AD1 — tRNA, 74 nt, 2 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 0
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
None — 0 exons
Expression profiles
Top tissues by expression
0 total, by Bgee expression score (0-100, higher = more expressed):
Regulation
Is transcription factor: no
Literature-anchored findings (GeneRIF, showing 12)
- results show that LK6 binds to ERK and is activated by ERK signalling and it is responsible for phosphorylating eIF4E in Drosophila (PMID:15487973)
- our results suggest that the level of eIF4E protein is regulated by Diap1, and that IAPs may play a role in cap-dependent translation by regulating the level of eIF4E protein. (PMID:18182863)
- These results suggest that the eIF4E-1,2 gene is regulated by Hfp through a mechanism linked to transcription control and 3’ splice site selection, which determines the pattern and translation efficiency of eIF4E-1,2 mRNAs. (PMID:18671938)
- data are consistent with the idea that Parkin and eIF4E act in a common pathway, likely modulating cap-dependent translation initiation events. (PMID:20869429)
- eIF4E regulates the sex-specific expression of the master switch gene Sxl. (PMID:21829374)
- Protein-protein interactions rather than interactions with the mRNA are essential for the recruitment of eIF4E and for a putative nucleation function. (PMID:22507384)
- Eukaryotic initiation factor 4E-3 is essential for meiotic chromosome segregation, cytokinesis and male fertility in Drosophila. (PMID:22833128)
- eIF4E-binding protein requires non-canonical 4E-binding motifs and a lateral surface of eIF4E to repress translation. (PMID:25179781)
- Phosphorylation of 4E-BP1 impairs the competition with eIF4G for eIF4E binding. (PMID:25702871)
- Both eIF4E-1 and eIF4E-3 are required in spermatocytes for chromosome condensation and cytokinesis during the meiotic stages. (PMID:25849588)
- The structures of eIF4E-eIF4G complexes reveal an extended interface to regulate translation initiation. (PMID:27773676)
- Drosophila Me31B is a Dual eIF4E-Interacting Protein. (PMID:36638908)
Cross-species orthologs
0 orthologs
Protein
Protein identifiers
Canonical reviewed UniProt: None (reviewed: )
All UniProt accessions (0):
RefSeq proteins (0): (*=MANE)
Domains & families (InterPro)
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 0 (showing top):
GO Biological Process (0):
GO Molecular Function (0):
GO Cellular Component (0):
Protein interactions and networks
STRING
0 interactions, top by confidence (×1000):
IntAct
0 interactions, top by confidence:
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
0 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 0 |
| Likely benign | 0 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
0 predictions. Top by Δscore:
AlphaMissense
0 scored. Top likely-pathogenic:
Disease associations
OMIM: gene `` | disease phenotypes:
GenCC curated gene-disease
Mondo (0):
Orphanet (0):
HPO phenotypes
0 total (0 of 0 shown, HPO-id order):
GWAS associations
0 associations (top):
Drugs & pharmacology
Drug and pharmacology data
Is drug target: no
PharmGKB: 0 entries
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.