Statements (24)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:gene
|
| gptkbp:associatedWith |
gptkb:GLUT1_deficiency_syndrome
epilepsy |
| gptkbp:biologicalProcess |
glucose transport
hexose transport |
| gptkbp:cellularComponent |
gptkb:plasma_membrane
|
| gptkbp:encodes |
gptkb:GLUT1
|
| gptkbp:Entrez_Gene_ID |
6513
|
| gptkbp:fullName |
gptkb:solute_carrier_family_2_member_1
|
| gptkbp:function |
glucose transporter activity
|
| gptkbp:gene |
gptkb:SLC2A1
|
| gptkbp:HGNC_ID |
11005
|
| https://www.w3.org/2000/01/rdf-schema#label |
ENSG00000108984
|
| gptkbp:locatedOnChromosome |
chromosome 1
|
| gptkbp:OMIM |
138140
|
| gptkbp:organism |
gptkb:Homo_sapiens
|
| gptkbp:strand |
plus
|
| gptkbp:UniProtID |
P11166
ENSP00000229239 |
| gptkbp:bfsParent |
gptkb:RAPGEF90
gptkb:MAP2K3 gptkb:MAP2K6 gptkb:MKK6 |
| gptkbp:bfsLayer |
7
|