| Gene | Input weight | Standard | Rank | |
| SLC1A2 | - | - | 119 | |
| SLC1A1 | 0.25 | 1 | 363 | |
| KCNJ10 | - | -1 | 733 | |
| CLN8 | - | -1 | 6415 | |
| SLC1A3 | 0.25 | 1 | 7455 | |
| SLC25A4 | - | -1 | 15900 |
GO:0051938
| Name | Description | External IDs |
| SLC1A2 | solute carrier family 1 (glial high affinity glutamate transporter), member 2 | Entrez:6506 Ensembl: ENSG00000110436 HGNC: 10940 HPRD: 02625 |
| SLC1A1 | solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1 | Entrez:6505 HPRD: 00597 HGNC: 10939 Ensembl: ENSG00000106688 |
| KCNJ10 | potassium inwardly-rectifying channel, subfamily J, member 10 | Entrez:3766 Ensembl: ENSG00000177807 HGNC: 6256 HPRD: 03732 |
| CLN8 | ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation) | Entrez:2055 Ensembl: ENSG00000182372 HGNC: 2079 HPRD: 06383 |
| SLC1A3 | solute carrier family 1 (glial high affinity glutamate transporter), member 3 | Entrez:6507 Ensembl: ENSG00000079215 HGNC: 10941 HPRD: 02523 |
| Geneset | Type | Freq. (Network vs Genome) | P-Value (FDR Corrected) | Genes |
| Gene | Description | Avg. edge score to query | Rank | In geneset | In query |
| SLC1A2 | solute carrier family 1 (glial high affinity glutamate transporter), member 2 | ||||
| SLC1A1 | solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1 | ||||
| KCNJ10 | potassium inwardly-rectifying channel, subfamily J, member 10 | ||||
| CLN8 | ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation) | ||||
| SLC1A3 | solute carrier family 1 (glial high affinity glutamate transporter), member 3 |
| Query gene | Gene | Gene description | Edge score |
| SLC1A2 | SLC1A2 | solute carrier family 1 (glial high affinity glutamate transporter), member 2 | |
| SLC1A1 | SLC1A1 | solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1 | |
| KCNJ10 | KCNJ10 | potassium inwardly-rectifying channel, subfamily J, member 10 | |
| CLN8 | CLN8 | ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation) | |
| SLC1A3 | SLC1A3 | solute carrier family 1 (glial high affinity glutamate transporter), member 3 |