SLC1A1

GENERAL INFORMATION

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Gene name

SLC1A1

Gene description

Solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1

Protein class

Disease related genes
Potential drug targets
Predicted membrane proteins
Transporters

Predicted localization

Membrane

Number of transcripts

2
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (small intestine)
GTEx:Tissue enhanced (small intestine)

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic expression in most cell types.

ANTIBODY RELIABILITY

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Data reliability
description

Pending RNA-based expert annotation.

Data reliability

Uncertain based on 2 antibodies.
HPA020086 , CAB015466
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis

Skin



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enhanced (small intestine)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (small intestine)

Organ

Expression



GENE INFORMATION

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Gene name

SLC1A1 (HGNC Symbol)

Synonyms

EAAC1, EAAT3

Description

Solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1 (HGNC Symbol)

Entrez gene summary

This gene encodes a member of the high-affinity glutamate transporters that play an essential role in transporting glutamate across plasma membranes. In brain, these transporters are crucial in terminating the postsynaptic action of the neurotransmitter glutamate, and in maintaining extracellular glutamate concentrations below neurotoxic levels. This transporter also transports aspartate, and mutations in this gene are thought to cause dicarboxylicamino aciduria, also known as glutamate-aspartate transport defect. [provided by RefSeq, Mar 2010]

Chromosome

9

Cytoband

p24.2

Chromosome location (bp)

4490444 - 4587469

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000106688 (version 78.38)

Entrez gene

6505

UniProt

P43005 (UniProt - Evidence at protein level)

neXtProt

NX_P43005

Antibodypedia

SLC1A1 antibodies


PROTEIN BROWSER

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ENST00000262352
 
ENST00000422398
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

SLC1A1-001 ENSP00000262352
ENST00000262352
P43005
Show all »
Show » Show » 524 57.1 No >9
SLC1A1-002 ENSP00000414620
ENST00000422398
Show » Show » 242 26.6 No 3