GO:0043092 L-amino acid import (8)

GeneInput weightStandardRank
SLC1A2--119
SLC6A10.251313
SLC1A10.251363
KCNJ10--1733
CLN8--16415
SLC1A30.2517455
SLC25A4--115900
SLC11A1--23561

Network

GO:0043092

Network
Enrichment
NameDescriptionExternal IDs
SLC1A2solute carrier family 1 (glial high affinity glutamate transporter), member 2 Entrez:6506  HPRD: 02625  HGNC: 10940  Ensembl: ENSG00000110436 
SLC6A1solute carrier family 6 (neurotransmitter transporter), member 1 Entrez:6529  HPRD: 00664  HGNC: 11042  Ensembl: ENSG00000157103 
SLC1A1solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1 Entrez:6505  HGNC: 10939  HPRD: 00597  Ensembl: ENSG00000106688 
KCNJ10potassium inwardly-rectifying channel, subfamily J, member 10 Entrez:3766  HPRD: 03732  HGNC: 6256  Ensembl: ENSG00000177807 
CLN8ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation) Entrez:2055  HPRD: 06383  HGNC: 2079  Ensembl: ENSG00000182372 
GenesetTypeFreq. (Network vs Genome)P-Value (FDR Corrected)Genes
GeneDescriptionAvg. edge score to queryRankIn genesetIn query
SLC1A2solute carrier family 1 (glial high affinity glutamate transporter), member 2
SLC6A1solute carrier family 6 (neurotransmitter transporter), member 1
SLC1A1solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1
KCNJ10potassium inwardly-rectifying channel, subfamily J, member 10
CLN8ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)
Query geneGeneGene descriptionEdge score
SLC1A2SLC1A2solute carrier family 1 (glial high affinity glutamate transporter), member 2
SLC6A1SLC6A1solute carrier family 6 (neurotransmitter transporter), member 1
SLC1A1SLC1A1solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1
KCNJ10KCNJ10potassium inwardly-rectifying channel, subfamily J, member 10
CLN8CLN8ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)