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Symbol
Name
ID
Slc2a1
solute carrier family 2 (facilitated glucose transporter), member 1
MGI:95755
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Lower limb spasticity
Spastic paraplegia
Paresthesia
Cerebral atrophy
Hypoglycorrhachia
Morphological abnormality of the pyramidal tract
EEG abnormality
Ataxia
Episodic ataxia
Abnormal pyramidal sign
Cognitive impairment
Intellectual disability
Intellectual disability, mild
Dysarthria
Hyperreflexia
Hyperactive deep tendon reflexes
Dyskinesia
Dystonia
Torsion dystonia
Involuntary movements
Chorea
Choreoathetosis
Paroxysmal dyskinesia
Tremor
Aggressive behavior
Irritability
Headache
Migraine
Global developmental delay
Specific learning disability
Seizures
Absence seizure
Generalized tonic-clonic seizures
Disease(s) Associated with SLC2A1
childhood onset GLUT1 deficiency syndrome 2
dystonia 9
idiopathic generalized epilepsy 12

Mouse Phenotypes
sporadic seizures
decreased brain weight
Availability Mouse Genotype
Slc2a1tm1Dcdv/Slc2a1+

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
11/05/2019
MGI 6.14
The Jackson Laboratory