Symbol
Name
ID

Slc6a1
solute carrier family 6 (neurotransmitter transporter, GABA), member 1
MGI:95627

Phenotype annotations related to nervous system

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes

Delayed CNS myelination

Ataxia

Eyelid myoclonus

Tremor

Autistic behavior

Addictive alcohol use

Attention deficit hyperactivity disorder

Intellectual disability

Global developmental delay

Generalized non-motor (absence) seizure

Generalized myoclonic-atonic seizure

Atonic seizure

Myoclonic seizure

Disease(s) Associated with SLC6A1

alcohol dependence

myoclonic-atonic epilepsy

Mouse Phenotypes		nervous system phenotype	reduced sensorimotor gating	abnormal GABA-mediated receptor currents	abnormal inhibitory postsynaptic currents	decreased prepulse inhibition	abnormal neurotransmitter secretion	abnormal neurotransmitter uptake
Availability	Mouse Genotype	nervous system phenotype	reduced sensorimotor gating	abnormal GABA-mediated receptor currents	abnormal inhibitory postsynaptic currents	decreased prepulse inhibition	abnormal neurotransmitter secretion	abnormal neurotransmitter uptake
	Slc6a1^tm1Lst/Slc6a1^tm1Lst
	Slc6a1^tm1Mlit/Slc6a1^tm1Mlit	*

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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