Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 189
MIM: 604285
HGNC: 341
Ensembl: ENSG00000172482
Variants:
dbSNP: 189
ClinVar: 189
TCGA: ENSG00000172482
COSMIC: AGXT
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000172482 | ENST00000307503 | P21549 |
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38243391 | 2024 | Insights into the pathogenesis of primary hyperoxaluria type I from the structural dynamics of alanine:glyoxylate aminotransferase variants. | 1 |
| 38657121 | 2024 | Expanding the Genetic Spectrum of AGXT Gene Variants in Egyptian Patients with Primary Hyperoxaluria Type I. | 0 |
| 38243391 | 2024 | Insights into the pathogenesis of primary hyperoxaluria type I from the structural dynamics of alanine:glyoxylate aminotransferase variants. | 1 |
| 38657121 | 2024 | Expanding the Genetic Spectrum of AGXT Gene Variants in Egyptian Patients with Primary Hyperoxaluria Type I. | 0 |
| 37874369 | 2023 | Case series and literature review of primary hyperoxaluria type 1 in Chinese patients. | 1 |
| 37874369 | 2023 | Case series and literature review of primary hyperoxaluria type 1 in Chinese patients. | 1 |
| 34995728 | 2022 | Extended genetic analysis of exome sequencing for primary hyperoxaluria in pediatric urolithiasis patients with hyperoxaluria. | 2 |
| 35661454 | 2022 | Next-generation sequencing in identification of pathogenic variants in primary hyperoxaluria among 21 Egyptian families: Identification of two novel AGXT gene mutations. | 3 |
| 34995728 | 2022 | Extended genetic analysis of exome sequencing for primary hyperoxaluria in pediatric urolithiasis patients with hyperoxaluria. | 2 |
| 35661454 | 2022 | Next-generation sequencing in identification of pathogenic variants in primary hyperoxaluria among 21 Egyptian families: Identification of two novel AGXT gene mutations. | 3 |
| 32556641 | 2021 | Characteristics of the genotype and phenotype in Chinese primary hyperoxaluria type 1 populations. | 3 |
| 33408043 | 2021 | Pharmacogenetics of advanced lung cancer: Predictive value of functional genetic polymorphism AGXT Pro11Leu in clinical outcome? | 2 |
| 32556641 | 2021 | Characteristics of the genotype and phenotype in Chinese primary hyperoxaluria type 1 populations. | 3 |
| 33408043 | 2021 | Pharmacogenetics of advanced lung cancer: Predictive value of functional genetic polymorphism AGXT Pro11Leu in clinical outcome? | 2 |
| 32569165 | 2020 | Primary hyperoxaluria Type 1: A case report in an extended family with a novel AGXT gene mutation. | 0 |
Citation
Dessen P
AGXT (alanine--glyoxylate and serine--pyruvate aminotransferase)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/60211/agxt-(alanine-glyoxylate-and-serine-pyruvate-aminotransferase)
