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- NCIT_C97684 IAO_0000115 "Human P2RY8 wild-type allele is located in the vicinity of Xp22.33 and Yp11.3 and is approximately 75 kb in length. This allele, which encodes P2Y purinoceptor 8 protein, is involved in G-protein coupled receptor signaling. A chromosomal deletion in the pseudoautosomal region 1 of either chromosome X or Y causing fusion of this gene with the CRLF2 gene is associated with B-cell acute lymphoblastic leukemia. Two pericentric inversions of the X chromosome inv(X)(q13;p22) and inv(X)(p22.3;q13.2) disrupt the gene and are associated with mental retardation." @default.
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- NCIT_C97684 NCIT_P106 "Gene or Genome" @default.
- NCIT_C97684 NCIT_P107 "P2RY8 wt Allele" @default.
- NCIT_C97684 NCIT_P108 "P2RY8 wt Allele" @default.
- NCIT_C97684 NCIT_P207 "C3273564" @default.
- NCIT_C97684 NCIT_P321 "286530" @default.
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- NCIT_C97684 hasExactSynonym "MGC50878" @default.
- NCIT_C97684 hasExactSynonym "P2RY8 wt Allele" @default.
- NCIT_C97684 hasExactSynonym "P2Y Receptor Family Member 8 wt Allele" @default.
- NCIT_C97684 hasExactSynonym "P2Y8" @default.
- NCIT_C97684 hasExactSynonym "Purinergic Receptor P2Y, G-Protein Coupled, 8 Gene" @default.
- NCIT_C97684 hasExactSynonym "Pyrimidinergic Receptor P2Y, G Protein-Coupled, 8 Gene" @default.
- NCIT_C97684 hasExactSynonym "RP11-261P4.4" @default.
- NCIT_C97684 inSubset NCIT_C116977 @default.
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- NCIT_C97684 type Class @default.
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- NCIT_C97684 label "P2RY8 wt Allele" @default.
- NCIT_C97684 subClassOf NCIT_C16612 @default.
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