Identity
HGNC
LOCATION
11p13
LOCUSID
ALIAS
DEE41,EAAT2,EIEE41,GLT-1,HBGT
FUSION GENES
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: 6506
MIM: 600300
HGNC: 10940
Ensembl: ENSG00000110436
Variants:
dbSNP: 6506
ClinVar: 6506
TCGA: ENSG00000110436
COSMIC: SLC1A2
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38086219 | 2024 | Leat-associated seizures the possible role of EAAT2, pyruvate carboxylase and glutamine synthetase. | 0 |
| 38690938 | 2024 | Hyperglycemia impairs EAAT2 glutamate transporter trafficking and glutamate clearance in islets of Langerhans: implications for type 2 diabetes pathogenesis and treatment. | 0 |
| 38086219 | 2024 | Leat-associated seizures the possible role of EAAT2, pyruvate carboxylase and glutamine synthetase. | 0 |
| 38690938 | 2024 | Hyperglycemia impairs EAAT2 glutamate transporter trafficking and glutamate clearance in islets of Langerhans: implications for type 2 diabetes pathogenesis and treatment. | 0 |
| 36173507 | 2023 | The role of excitatory amino acid transporter 2 (EAAT2) in epilepsy and other neurological disorders. | 4 |
| 37178383 | 2023 | The Regulation of GLT-1 Degradation Pathway by SIRT4. | 0 |
| 36173507 | 2023 | The role of excitatory amino acid transporter 2 (EAAT2) in epilepsy and other neurological disorders. | 4 |
| 37178383 | 2023 | The Regulation of GLT-1 Degradation Pathway by SIRT4. | 0 |
| 34961934 | 2022 | Mutations associated with epileptic encephalopathy modify EAAT2 anion channel function. | 7 |
| 35260124 | 2022 | Polymorphism of rs12294045 in EAAT2 gene is potentially associated with schizophrenia in Chinese Han population. | 2 |
| 35318310 | 2022 | PKCα phosphorylation of GLT-1 at Ser562/563 induces glutamate excitotoxicity in ischemia in mice. | 3 |
| 35953475 | 2022 | Structural insights into inhibitory mechanism of human excitatory amino acid transporter EAAT2. | 10 |
| 34961934 | 2022 | Mutations associated with epileptic encephalopathy modify EAAT2 anion channel function. | 7 |
| 35260124 | 2022 | Polymorphism of rs12294045 in EAAT2 gene is potentially associated with schizophrenia in Chinese Han population. | 2 |
| 35318310 | 2022 | PKCα phosphorylation of GLT-1 at Ser562/563 induces glutamate excitotoxicity in ischemia in mice. | 3 |
Citation
Dessen P
SLC1A2 (solute carrier family 1 member 2)
Atlas Genet Cytogenet Oncol Haematol. 2011-08-01
Online version: http://atlasgeneticsoncology.org/gene/52325/slc1a2
