Statements (23)
Predicate | Object |
---|---|
gptkbp:instanceOf |
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
|
https://www.w3.org/2000/01/rdf-schema#label |
ENSG00000168137
|
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 |
7
|