Statements (41)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:Ensembl_gene_ID
|
| gptkbp:alternativeName |
gptkb:GLUT1
|
| gptkbp:associatedGeneName |
gptkb:SLC2A1
|
| gptkbp:associatedWith |
gptkb:GLUT1_deficiency_syndrome
epilepsy hereditary stomatocytosis |
| gptkbp:encodes |
gptkb:solute_carrier_family_2_member_1
|
| gptkbp:geneType |
protein-coding
|
| gptkbp:hasTranscript |
ENST00000381652
ENST00000423562 ENST00000436094 ENST00000439321 ENST00000440486 ENST00000441781 ENST00000442987 ENST00000443713 ENST00000444446 ENST00000444811 ENST00000445313 ENST00000445713 ENST00000446013 ENST00000446413 ENST00000446813 ENST00000447213 ENST00000447613 ENST00000448013 ENST00000448413 ENST00000448813 ENST00000449213 |
| gptkbp:HGNC_ID |
11005
|
| gptkbp:locatedOnChromosome |
chromosome 1
43396441 43412609 |
| gptkbp:OMIM |
138140
|
| gptkbp:organism |
gptkb:Homo_sapiens
|
| gptkbp:referenceGenome |
gptkb:GRCh38
|
| gptkbp:strand |
plus
|
| gptkbp:UniProtID |
P11166
|
| gptkbp:bfsParent |
gptkb:CD277
|
| gptkbp:bfsLayer |
8
|
| https://www.w3.org/2000/01/rdf-schema#label |
ENSG00000186470
|