solute carrier family 2 member 1
GPTKB entity
Statements (29)
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
|
https://www.w3.org/2000/01/rdf-schema#label |
solute carrier family 2 member 1
|
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:SLC2A1
|
gptkbp:bfsLayer |
7
|