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- NCIT_C92670 IAO_0000115 "Human SLC1A2 wild-type allele is located within 11p13-p12 and is approximately 169 kb in length. This allele, which encodes excitatory amino acid transporter 2 protein, is involved in the regulation of both amino acid transport and synaptic transmission. Mutation and deletion of the gene are associated with amyotrophic lateral sclerosis." @default.
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- NCIT_C92670 NCIT_P102 "AB209444" @default.
- NCIT_C92670 NCIT_P106 "Gene or Genome" @default.
- NCIT_C92670 NCIT_P108 "SLC1A2 wt Allele" @default.
- NCIT_C92670 NCIT_P207 "C2985245" @default.
- NCIT_C92670 NCIT_P321 "6506" @default.
- NCIT_C92670 NCIT_P98 "Defects in the SLC1A2 gene may be associated with migraine." @default.
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- NCIT_C92670 NCIT_R40 NCIT_C34070 @default.
- NCIT_C92670 NCIT_R41 NCIT_C14182 @default.
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- NCIT_C92670 NCIT_R41 NCIT_C14262 @default.
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- NCIT_C92670 NCIT_R41 NCIT_C25796 @default.
- NCIT_C92670 NCIT_R41 NCIT_C79740 @default.
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- NCIT_C92670 referenceCount "1" @default.
- NCIT_C92670 hasExactSynonym "DEE41" @default.
- NCIT_C92670 hasExactSynonym "EAAT2" @default.
- NCIT_C92670 hasExactSynonym "EIEE41" @default.
- NCIT_C92670 hasExactSynonym "Excitotoxic Amino Acid Transporter 2 Gene" @default.
- NCIT_C92670 hasExactSynonym "GLT-1" @default.
- NCIT_C92670 hasExactSynonym "GLT1" @default.
- NCIT_C92670 hasExactSynonym "Glial High Affinity Glutamate Transporter Gene" @default.
- NCIT_C92670 hasExactSynonym "HBGT" @default.
- NCIT_C92670 hasExactSynonym "SLC1A2 wt Allele" @default.
- NCIT_C92670 hasExactSynonym "Solute Carrier Family 1 (Glial High Affinity Glutamate Transporter), Member 2 Gene" @default.
- NCIT_C92670 hasExactSynonym "Solute Carrier Family 1 Member 2 wt Allele" @default.
- NCIT_C92670 type Class @default.
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- NCIT_C92670 label "SLC1A2 wt Allele" @default.
- NCIT_C92670 subClassOf NCIT_C16612 @default.
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