Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:Ensembl_gene_ID
|
| gptkbp:alternativeName |
gptkb:solute_carrier_family_2_member_1
|
| gptkbp:associatedWith |
gptkb:GLUT1_deficiency_syndrome
gptkb:hereditary_spastic_paraplegia epilepsy |
| gptkbp:encodes |
gptkb:GLUT1
|
| gptkbp:Entrez_Gene_ID |
6513
ENSP00000264721 |
| gptkbp:gene |
gptkb:SLC2A1
|
| gptkbp:geneType |
protein_coding
|
| gptkbp:hasRefSeqID |
gptkb:NM_006516
|
| gptkbp:hasTranscript |
ENST00000264721
|
| gptkbp:HGNC_ID |
11005
|
| gptkbp:locatedOnChromosome |
chromosome 1
|
| gptkbp:OMIM |
138140
|
| gptkbp:organism |
gptkb:Homo_sapiens
|
| gptkbp:startPoint |
42923781
42959833 |
| gptkbp:strand |
plus
|
| gptkbp:UniProtID |
P11166
|
| gptkbp:bfsParent |
gptkb:SESN2
|
| gptkbp:bfsLayer |
8
|
| http://www.w3.org/2000/01/rdf-schema#label |
ENSG00000168137
|