Statements (27)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
Ensembl gene ID
|
| gptkbp:alternativeName |
gptkb:solute_carrier_family_2_member_1
|
| gptkbp:associatedWith |
gptkb:GLUT1_deficiency_syndrome
epilepsy hereditary stomatocytosis |
| gptkbp:encodes |
gptkb:GLUT1
|
| gptkbp:Entrez_Gene_ID |
6513
|
| gptkbp:gene |
gptkb:SLC2A1
|
| gptkbp:geneType |
protein-coding
|
| gptkbp:hasRefSeqID |
gptkb:NM_006516
|
| gptkbp:hasTranscript |
ENST00000381652
ENST00000423562 |
| gptkbp:HGNC_ID |
HGNC:11005
|
| https://www.w3.org/2000/01/rdf-schema#label |
ENSG00000164362
|
| gptkbp:locatedOnChromosome |
chromosome 1
43396441 43415734 |
| gptkbp:OMIM |
138140
|
| gptkbp:organism |
gptkb:Homo_sapiens
|
| gptkbp:strand |
plus
|
| gptkbp:UniProtID |
P11166
|
| gptkbp:bfsParent |
gptkb:FBgn0001624
gptkb:FBgn0002716 gptkb:FBgn0003079 gptkb:FBgn0003366 gptkb:TERT |
| gptkbp:bfsLayer |
8
|