Version: 8.2.0
Date: Wed Aug 27 2025
70 results for glt-7

glt-7

(Caenorhabditis elegans)
Gene
Name: GLutamate Transporter family 7
Synonyms: W03G1.1, CELE_W03G1.1
Source: WB:WBGene00001625
Biotype: protein coding gene
Symbol: glt-7 (Cel)
Symbol: glt-7
Cross References: WB:glt-7...glt-7...glt-7

SLC1A2

(Homo sapiens)
Gene
Name: solute carrier family 1 member 2
Synonyms: sodium-dependent glutamate/aspartate transporter 2, EIEE41, GLT1, HBGT, solute carrier family 1 (glial high affinity glutamate transporter), member 2, EAAT2, excitatory amino acid transporter 2, excitotoxic amino acid transporter 2, glutamate transporter-1, glutamate/aspartate transporter II, glial high affinity glutamate transporter, solute carrier family 1, member 2, human brain glutamate transporter, GLT-1, DEE41
Source: HGNC:10940
Biotype: protein coding gene
Strict Orthology Symbols: glt-7

Slc1a2

(Rattus norvegicus)
Gene
Name: solute carrier family 1 member 2
Synonyms: glutamate transporter 1, sodium-dependent glutamate/aspartate transporter 2, GluT, glial glutamate transporter GLT1/V1, solute carrier family 1 (glial high affinity glutamate transporter), member 2, excitatory amino acid transporter 2, Glt, glutamate transporter, glial glutamate transporter GLT1/V4, glial glutamate transporter GLT1/V3, glial glutamate transporter GLT1/V2, GluT-R, high affinity glucose transporter, Eaat2, solute carrier family 1, member 2, GLT-1
Source: RGD:3697
Biotype: protein coding gene
Strict Orthology Symbols: glt-7

Eaat2

(Drosophila melanogaster)
Gene
Name: Excitatory amino acid transporter 2
Synonyms: dEAAT2, dEaat2, Eaat 2, CG3159, sodium-dependent excitatory amino acid transporter 2, EAAT2, excitatory amino acid transporter 2, EAAT
Source: FB:FBgn0026438
Biotype: protein coding gene
Strict Orthology Symbols: glt-7

tm1641

(Caenorhabditis elegans)
Allele/Variant
Source: WB:WBVar00250620
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: glt-7 (Cel)

developmental and epileptic encephalopathy 41

Disease
Source: DOID:0080442
Definition: A developmental and epileptic encephalopathy characterized by onset in the first days or weeks of life of seizures, severely impaired psychomotor development, and brain anomalies including delayed myelination, thin corpus callosum, and cerebral atrophy that has_material_basis_in heterozygous mutation in the SLC1A2 gene on chromosome 11p13.
Genes: glt-7 (Cel)

glutamate:sodium symporter activity

Gene Ontology
Source: GO:0015501
Synonyms:
  • sodium/excitatory glutamate cotransporter activity
  • sodium/excitatory glutamate symporter activity
Branch: molecular function
Genes: glt-7 (Cel)

L-alpha-amino acid transmembrane transport

Gene Ontology
Source: GO:1902475
Synonyms: Not Available
Branch: biological process
Genes: glt-7 (Cel)

neutral amino acid transport

Gene Ontology
Source: GO:0015804
Synonyms: Not Available
Branch: biological process
Genes: glt-7 (Cel)

L-glutamate transmembrane transporter activity

Gene Ontology
Source: GO:0005313
Synonyms:
  • L-glutamate transporter activity
  • glutamate transmembrane transporter activity
Branch: molecular function
Genes: glt-7 (Cel)

neutral L-amino acid transmembrane transporter activity

Gene Ontology
Source: GO:0015175
Synonyms:
  • neutral amino acid transmembrane transporter activity
  • neutral amino acid transporter activity
Branch: molecular function
Genes: glt-7 (Cel)

L-glutamate transmembrane transport

Gene Ontology
Source: GO:0015813
Synonyms:
  • L-glutamate transport
  • mitochondrial aspartate/glutamate transport
Branch: biological process
Genes: glt-7 (Cel)

symporter activity

Gene Ontology
Source: GO:0015293
Synonyms:
  • cotransporter activity
  • porter activity
Branch: molecular function
Genes: glt-7 (Cel)

nicotine dependence

Disease
Source: DOID:0050742
Definition: A substance dependence that is characterized by a physical dependence on nicotine.
Genes: glt-7 (Cel)

amyotrophic lateral sclerosis

Disease
Source: DOID:332
Definition: A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing.
Genes: glt-7 (Cel)

Huntington's disease

Disease
Source: DOID:12858
Definition: A neurodegenerative disease that has_material_basis_in autosomal dominant inheritance and is characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia and has_material_basis_in expansion of CAG triplet repeats (glutamine) resulting in neuron degeneration affecting muscle coordination, cognitive abilities.
Genes: glt-7 (Cel)

middle cerebral artery infarction

Disease
Source: DOID:3525
Definition: Not Available
Genes: glt-7 (Cel)

alcohol dependence

Disease
Source: DOID:0050741
Definition: A substance dependence that is characterized by tolerance, withdrawal symptoms, increasing use, persistent desire to decrease consumption, time spent obtaining or recovering from alcohol caused by a physical and psychological dependence on alcohol.
Genes: glt-7 (Cel)

alcohol use disorder

Disease
Source: DOID:1574
Definition: A substance abuse that involves the recurring use of alcoholic beverages despite negative consequences.
Genes: glt-7 (Cel)

Alzheimer's disease

Disease
Source: DOID:10652
Definition: A tauopathy that is characterized by memory lapses, confusion, emotional instability and progressive loss of mental ability and results in progressive memory loss, impaired thinking, disorientation, and changes in personality and mood starting and leads in advanced cases to a profound decline in cognitive and physical functioning and is marked histologically by the degeneration of brain neurons especially in the cerebral cortex and by the presence of neurofibrillary tangles and plaques containing beta-amyloid.
Genes: glt-7 (Cel)

(WBcel235)IV:534324C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.534324C>T
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:534324C>T
Gene Cross References: glt-7

(WBcel235)IV:535225C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.535225C>T
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:535225C>T
Gene Cross References: glt-7

(WBcel235)IV:532837T>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.532837T>C
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:532837T>C
Gene Cross References: glt-7

(WBcel235)IV:534795G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.534795G>A
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:534795G>A
Gene Cross References: glt-7

(WBcel235)IV:533813C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.533813C>T
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:533813C>T
Gene Cross References: glt-7

(WBcel235)IV:533861G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.533861G>A
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:533861G>A
Gene Cross References: glt-7

(WBcel235)IV:532451A>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.532451A>C
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:532451A>C
Gene Cross References: glt-7

(WBcel235)IV:533216C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.533216C>T
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:533216C>T
Gene Cross References: glt-7

(WBcel235)IV:534471C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.534471C>T
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:534471C>T
Gene Cross References: glt-7

(WBcel235)IV:532548C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.532548C>T
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:532548C>T
Gene Cross References: glt-7

(WBcel235)IV:532325C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.532325C>T
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:532325C>T
Gene Cross References: glt-7

(WBcel235)IV:533117G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.533117G>A
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:533117G>A
Gene Cross References: glt-7

(WBcel235)IV:533576C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.533576C>T
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:533576C>T
Gene Cross References: glt-7

(WBcel235)IV:532566C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.532566C>T
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:532566C>T
Gene Cross References: glt-7

(WBcel235)IV:534092G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.534092G>A
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:534092G>A
Gene Cross References: glt-7

(WBcel235)IV:535077G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.535077G>A
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:535077G>A
Gene Cross References: glt-7

(WBcel235)IV:533227A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.533227A>G
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:533227A>G
Gene Cross References: glt-7

(WBcel235)IV:533136A>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.533136A>C
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:533136A>C
Gene Cross References: glt-7

(WBcel235)IV:534526G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.534526G>A
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:534526G>A
Gene Cross References: glt-7

(WBcel235)IV:535065G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.535065G>A
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:535065G>A
Gene Cross References: glt-7

(WBcel235)IV:533081A>G

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.533081A>G
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:533081A>G
Gene Cross References: glt-7

(WBcel235)IV:533228C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.533228C>T
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:533228C>T
Gene Cross References: glt-7

(WBcel235)IV:534528A>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.534528A>T
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:534528A>T
Gene Cross References: glt-7

(WBcel235)IV:532456G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.532456G>A
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:532456G>A
Gene Cross References: glt-7

(WBcel235)IV:532655C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.532655C>T
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:532655C>T
Gene Cross References: glt-7

(WBcel235)IV:534827C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.534827C>T
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:534827C>T
Gene Cross References: glt-7

(WBcel235)IV:535145T>C

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.535145T>C
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:535145T>C
Gene Cross References: glt-7

(WBcel235)IV:535192T>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.535192T>A
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:535192T>A
Gene Cross References: glt-7

(WBcel235)IV:533808G>A

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.533808G>A
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:533808G>A
Gene Cross References: glt-7

(WBcel235)IV:533902C>T

(Caenorhabditis elegans)
Allele/Variant
Source: NC_003282.8:g.533902C>T
Genes: glt-7 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)IV:533902C>T
Gene Cross References: glt-7