# Glycyl-tRNA synthetase 1

> mammalian protein found in Homo sapiens

**Wikidata**: [Q5572591](https://www.wikidata.org/wiki/Q5572591)  
**Source**: https://4ort.xyz/entity/glycyl-trna-synthetase-1


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/P41250)
3. Q20641742
4. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P41250)
5. [Crystal structure of human wildtype and S581L‐mutant glycyl‐tRNA synthetase, an enzyme underlying distal spinal muscular atrophy](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P41250)
6. [Long-range structural effects of a Charcot–Marie–Tooth disease-causing mutation in human glycyl-tRNA synthetase](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P41250)
7. [Crystal Structures and Biochemical Analyses Suggest a Unique Mechanism and Role for Human Glycyl-tRNA Synthetase in Ap4A Homeostasis](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P41250)
8. [Charcot–Marie–Tooth disease-associated mutant tRNA synthetases linked to altered dimer interface and neurite distribution defect](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P41250)
9. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=P41250&geneProductId=UniProtKB:P41250)
10. [Compound heterozygosity for loss-of-functionGARSvariants results in a multisystem developmental syndrome that includes severe growth retardation](http://www.ebi.ac.uk/QuickGO/annotations?protein=P41250&geneProductId=UniProtKB:P41250)
11. [Long-range structural effects of a Charcot–Marie–Tooth disease-causing mutation in human glycyl-tRNA synthetase](http://www.ebi.ac.uk/QuickGO/annotations?protein=P41250&geneProductId=UniProtKB:P41250)
12. [Crystal Structures and Biochemical Analyses Suggest a Unique Mechanism and Role for Human Glycyl-tRNA Synthetase in Ap4A Homeostasis](http://www.ebi.ac.uk/QuickGO/annotations?protein=P41250&geneProductId=UniProtKB:P41250)
13. [Crystal structure of human wildtype and S581L‐mutant glycyl‐tRNA synthetase, an enzyme underlying distal spinal muscular atrophy](http://www.ebi.ac.uk/QuickGO/annotations?protein=P41250&geneProductId=UniProtKB:P41250)
14. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?protein=P41250&geneProductId=UniProtKB:P41250)
15. [Compound heterozygosity for loss-of-functionGARSvariants results in a multisystem developmental syndrome that includes severe growth retardation](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P41250)
16. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P41250)
17. [Functional Analyses of Glycyl-tRNA Synthetase Mutations Suggest a Key Role for tRNA-Charging Enzymes in Peripheral Axons](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P41250)
18. [Proteomic analysis of podocyte exosome-enriched fraction from normal human urine](http://www.ebi.ac.uk/QuickGO/annotations?protein=P41250&geneProductId=UniProtKB:P41250)
19. [Primary structure and functional expression of human Glycyl-tRNA synthetase, an autoantigen in myositis](http://www.ebi.ac.uk/QuickGO/annotations?protein=P41250&geneProductId=UniProtKB:P41250)
20. [Primary structure and functional expression of human Glycyl-tRNA synthetase, an autoantigen in myositis](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:P41250)
21. Ensembl Release 99
22. Identifiers.org
23. UMLS 2023