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Symbol
Name
ID

Slc1a2
solute carrier family 1 (glial high affinity glutamate transporter), member 2
MGI:101931

Phenotype annotations related to behavior/neurological

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

Human Phenotypes	Feeding difficulties	Lethargy
Disease(s) Associated with SLC1A2	Feeding difficulties	Lethargy
developmental and epileptic encephalopathy 41

Mouse Phenotypes		behavior/neurological phenotype	increased susceptibility to pharmacologically induced seizures	hyperactivity	seizures	convulsive seizures
Availability	Mouse Genotype	behavior/neurological phenotype		hyperactivity	seizures	convulsive seizures
	Slc1a2^tm1Kta/Slc1a2^tm1Kta
	Slc1a2^tm1.1Ncd/Slc1a2^tm1.1Ncd Tg(Nes-cre)1Kln/0 (conditional)
	Slc1a2^tm1.1Pros/Slc1a2^tm1.1Pros Tg(GFAP-cre/ERT2)13Kdmc/0 (conditional)	*
	Slc1a2^tm1.1Pros/Slc1a2^tm1.1Pros Tg(Syn1-cre)671Jxm/0 (conditional)	*

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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