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- NCIT_C102459 IAO_0000115 "Human GRIN2B wild-type allele is located in the vicinity of 12p12 and is approximately 419 kb in length. This allele, which encodes glutamate receptor ionotropic, NMDA 2B protein, is involved in both glutamate binding and calcium transport. Mutation of the gene and chromosomal translocations involving the gene, t(9;12)(p23;p13.1) and t(10;12)(q21.1;p13.1), are associated with mental retardation." @default.
- NCIT_C102459 NCIT_NHC0 "C102459" @default.
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- NCIT_C102459 NCIT_P102 "NM_000834" @default.
- NCIT_C102459 NCIT_P106 "Gene or Genome" @default.
- NCIT_C102459 NCIT_P108 "GRIN2B wt Allele" @default.
- NCIT_C102459 NCIT_P207 "C3538769" @default.
- NCIT_C102459 NCIT_P321 "2904" @default.
- NCIT_C102459 NCIT_P98 "Mutation of the GRIN2B gene may be associated with autism. (Nature. 2012; 485:246-250.)" @default.
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- NCIT_C102459 hasExactSynonym "EIEE27" @default.
- NCIT_C102459 hasExactSynonym "GRIN2B wt Allele" @default.
- NCIT_C102459 hasExactSynonym "GluN2B" @default.
- NCIT_C102459 hasExactSynonym "Glutamate Receptor, Ionotropic, N-Methyl D-Aspartate 2B wt Allele" @default.
- NCIT_C102459 hasExactSynonym "Glutamate Receptor, Ionotropic, N-Methyl-D-Aspartate 2B Gene" @default.
- NCIT_C102459 hasExactSynonym "MGC142178" @default.
- NCIT_C102459 hasExactSynonym "MGC142180" @default.
- NCIT_C102459 hasExactSynonym "MRD6" @default.
- NCIT_C102459 hasExactSynonym "NMDAR2B" @default.
- NCIT_C102459 hasExactSynonym "NR2B" @default.
- NCIT_C102459 hasExactSynonym "hNR3" @default.
- NCIT_C102459 type Class @default.
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- NCIT_C102459 label "GRIN2B wt Allele" @default.
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