Preferred Label : glucose transporter type 1;
MeSH definition : A ubiquitously expressed glucose transporter that is important for constitutive, basal
GLUCOSE transport. It is predominately expressed in ENDOTHELIAL CELLS and ERYTHROCYTES
at the BLOOD-BRAIN BARRIER and is responsible for GLUCOSE entry into the BRAIN.;
MeSH synonym : glut-1 protein; solute carrier family 2, facilitated glucose transporter, member 1 protein; slc2a1 protein; erythrocyte glucose transporter; glut1 protein; glucose transporter, erythrocyte; glut 1 protein;
Is substance : O;
Origin ID : D051272;
UMLS CUI : C0168458;
Allowable qualifiers
Automatic exact mappings (from CISMeF team)
Indexing information
- WZB117 [MeSH Supplementary Concept]
Record concept(s)
Related MeSH Supplementary Concept(s)
Semantic type(s)
A ubiquitously expressed glucose transporter that is important for constitutive, basal
GLUCOSE transport. It is predominately expressed in ENDOTHELIAL CELLS and ERYTHROCYTES
at the BLOOD-BRAIN BARRIER and is responsible for GLUCOSE entry into the BRAIN.
https://www.has-sante.fr/jcms/p_3555046/fr/deficit-en-transporteur-de-glucose-glut1
2024
France
practice guideline
glucose transporter type 1
glucose, nos
chronic disease, nos
glucose
chronic disease
glucose
Handbook
---
https://www.has-sante.fr/jcms/p_3424746/fr/evaluation-du-test-metaglut1-dans-le-diagnostic-de-l-encephalopathie-par-deficit-en-transporteur-de-glucose-de-type-1
2023
France
health technology assessment
Encephalopathy
no diagnosis
glucose, nos
brain diseases
diagnosis
glucose
evaluation studies as topic
encephalopathy, nos
glucose transporter type 1
dermatomyositis
Glucose
---
https://asdglut1.wixsite.com/asdglut1
false
false
false
France
French
association of patients
glucose transporter type 1
---
https://anpgm.fr/media/documents/ANPGM_098_Deficit_en_GLUT1.doc
2012
France
guideline
Disease
disease, nos
Diseases
Glut1 Deficiency Syndrome
glucose transporter type 1
Diseases Category
Glut1 Deficiency Syndrome
carbohydrate metabolism, inborn errors
monosaccharide transport proteins
---
http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=71277
France
French
brain diseases
rare diseases
glucose transporter type 1
scientific and technical information
---
https://saez.swisshealthweb.ch/fr/article/doi/sanp.2011.02219
2011
false
true
false
Switzerland
Glut1 Deficiency Syndrome
carbohydrate metabolism, inborn errors
carbohydrate metabolism, inborn errors
carbohydrate metabolism, inborn errors
carbohydrate metabolism, inborn errors
carbohydrate metabolism, inborn errors
journal article
glucose transporter type 1
monosaccharide transport proteins
---