SLC1A3
Excitatory amino acid transporter 1
Also known as: EA6, EAA1_HUMAN, EAAT1, GLAST, GLAST-1, GLAST1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P43003
- Gene
- SLC1A3
- Ensembl
- ENSG00000079215
- Chromosome
- 5
- Canonical length
- 542 aa
- Protein class
- Cancer-related genes, Disease related genes, Human disease related genes, Metabolic proteins, Plasma proteins, Potential drug targets, Predicted intracellular proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Nucleoli,Vesicles
- Quaternary structure
- Homotrimer
OverviewNCBI Gene
This gene encodes a member of a member of a high affinity glutamate transporter family. This gene functions in the termination of excitatory neurotransmission in central nervous system. Mutations are associated with episodic ataxia, Type 6. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Feb 2014]
Canonical amino-acid sequenceUniProt
542 residues, UniProt reviewed canonical sequence.
>P43003|SLC1A3
1 MTKSNGEEPK MGGRMERFQQ GVRKRTLLAK KKVQNITKED VKSYLFRNAF VLLTVTAVIV
61 GTILGFTLRP YRMSYREVKY FSFPGELLMR MLQMLVLPLI ISSLVTGMAA LDSKASGKMG
121 MRAVVYYMTT TIIAVVIGII IVIIIHPGKG TKENMHREGK IVRVTAADAF LDLIRNMFPP
181 NLVEACFKQF KTNYEKRSFK VPIQANETLV GAVINNVSEA METLTRITEE LVPVPGSVNG
241 VNALGLVVFS MCFGFVIGNM KEQGQALREF FDSLNEAIMR LVAVIMWYAP VGILFLIAGK
301 IVEMEDMGVI GGQLAMYTVT VIVGLLIHAV IVLPLLYFLV TRKNPWVFIG GLLQALITAL
361 GTSSSSATLP ITFKCLEENN GVDKRVTRFV LPVGATINMD GTALYEALAA IFIAQVNNFE
421 LNFGQIITIS ITATAASIGA AGIPQAGLVT MVIVLTSVGL PTDDITLIIA VDWFLDRLRT
481 TTNVLGDSLG AGIVEHLSRH ELKNRDVEMG NSVIEENEMK KPYQLIAQDN ETEKPIDSET
541 KMLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SLC1A3 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Cell surface
- Secreted
- No
- Transmembrane segments
- 8
- Mean surface accessibility (rSASA)
- 0.3
- Highest tissue expression
- 527 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 527 nTPM
- amygdala: 472 nTPM
- basal ganglia: 455 nTPM
- hippocampal formation: 269 nTPM
- cerebellum: 248 nTPM
- midbrain: 219 nTPM
Single-cell type
- bergmann glia: 5,598 nCPM
- astrocytes: 2,442 nCPM
- microglia: 1,557 nCPM
- ependymal cells: 1,345 nCPM
- pituicytes/fscs: 1,168 nCPM
- müller glia: 1,040 nCPM
Immune cell
- myeloid DC: 1.6 nTPM
- classical monocyte: 1.5 nTPM
- intermediate monocyte: 1.2 nTPM
- total PBMC: 0.2 nTPM
- non-classical monocyte: 0.1 nTPM
- basophil: 0 nTPM
Brain region
- cerebral cortex: 456 nTPM
- cerebellum: 381 nTPM
- basal ganglia: 370 nTPM
- thalamus: 350 nTPM
- midbrain: 304 nTPM
- medulla oblongata: 290 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about SLC1A3.
Disease | AllUniProt
Conditions SLC1A3 is implicated in, by any mechanism.
- Episodic ataxia 6 (EA6) MIM:612656
Disease | GeneticClinVar
2 pathogenic / likely-pathogenic of 334 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Episodic ataxia type 6
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.28
- gnomAD pLI
- 0.99
- gnomAD missense Z
- 1.79
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- auditory behavior
- cell morphogenesis involved in neuron differentiation
- cellular response to cocaine
- chemical synaptic transmission
- chloride transmembrane transport
- cranial nerve development
- D-aspartate import across plasma membrane
- gamma-aminobutyric acid biosynthetic process
- intracellular sodium ion homeostasis
- L-aspartate import across plasma membrane
- L-glutamate import
- L-glutamate import across plasma membrane
- L-glutamate transmembrane transport
- monoatomic ion transport
- neuromuscular process controlling balance
- neurotransmitter transport
- neurotransmitter uptake
- positive regulation of synaptic transmission
- potassium ion transmembrane transport
- response to antibiotic
- response to light stimulus
- response to wounding
- response to xenobiotic stimulus
- sensory perception of sound
- transepithelial transport
- transport across blood-brain barrier
Molecular functions
- glutamate binding
- glutamate:sodium symporter activity
- high-affinity L-glutamate transmembrane transporter activity
- L-glutamate transmembrane transporter activity
- metal ion binding
- neutral L-amino acid transmembrane transporter activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SLC1A3 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SLC1A3 as an antibody target. Whether an autoantibody or antibody against SLC1A3 could matter depends on whether native SLC1A3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SLC1A3 is annotated at the cell surface, where native SLC1A3 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label SLC1A3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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