solute carrier family 2 member 1
GPTKB entity
Statements (33)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:protein
gptkb:gene |
| gptkbp:alsoKnownAs |
gptkb:GLUT1
gptkb:SLC2A1 |
| gptkbp:associatedWith |
gptkb:GLUT1_deficiency_syndrome
epilepsy hereditary stomatocytosis |
| gptkbp:encodedBy |
gptkb:SLC2A1_gene
|
| gptkbp:Entrez_Gene_ID |
6513
|
| gptkbp:expressedIn |
gptkb:blood-brain_barrier
erythrocytes |
| gptkbp:foundIn |
gptkb:Homo_sapiens
|
| gptkbp:function |
facilitated glucose transporter
|
| gptkbp:HGNC_ID |
11005
|
| gptkbp:length |
492
|
| gptkbp:locatedOnChromosome |
gptkb:1p34.2
chromosome 1 |
| gptkbp:memberOf |
gptkb:solute_carrier_family_2
|
| gptkbp:molecularWeight |
54 kDa
|
| gptkbp:OMIM |
138140
|
| gptkbp:orthologInMouse |
gptkb:Slc2a1
|
| gptkbp:structureType |
integral membrane protein
|
| gptkbp:transmembraneDomains |
12
|
| gptkbp:transportSubstrate |
gptkb:dehydroascorbic_acid
glucose |
| gptkbp:UniProtID |
P11166
|
| gptkbp:bfsParent |
gptkb:ENSG00000179218
gptkb:ENSG00000108984 gptkb:GLUT1 gptkb:SLC2A1 gptkb:SLC2A1_gene |
| gptkbp:bfsLayer |
8
|
| https://www.w3.org/2000/01/rdf-schema#label |
solute carrier family 2 member 1
|