TRG-CCC3-1
gene geneOn this page
Also known as tRNA-Gly-CCC-3-1
Summary
TRG-CCC3-1 (tRNA-Gly (anticodon CCC) 3-1, HGNC:34841) is a gene on chromosome 17p11.2.
At a glance
- Clinical variants (ClinVar): 2 total — 2 pathogenic
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:34841 |
| Approved symbol | TRG-CCC3-1 |
| Name | tRNA-Gly (anticodon CCC) 3-1 |
| Location | 17p11.2 |
| Locus type | RNA, transfer |
| Status | Approved |
| Aliases | tRNA-Gly-CCC-3-1 |
| Entrez | 100189277 |
| RNAcentral | URS0000684E4B — tRNA, 71 nt, 4 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
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
2 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 2 |
| Likely pathogenic | 0 |
| Uncertain significance | 0 |
| Likely benign | 0 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (2)
| Variant ID | HGVS | Classification |
|---|---|---|
| 150379 | GRCh38/hg38 17p11.2(chr17:16989087-20370816)x1 | Pathogenic |
| 155110 | GRCh38/hg38 17p12-11.2(chr17:15883037-20658018)x1 | Pathogenic |
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.