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- NCIT_C97550 IAO_0000115 "Human FOXP1 wild-type allele is located in the vicinity of 3p14.1 and is approximately 629 kb in length. This allele, which encodes forkhead box protein P1, plays a role in the negative regulation of transcription. Mutation of the gene is associated with mental retardation with language impairment and autistic features. A translocation t(9;3)(p13;p14.1) of this gene with the PAX5 gene is associated with acute lymphoblastic leukemia." @default.
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- NCIT_C97550 hasExactSynonym "12CC4" @default.
- NCIT_C97550 hasExactSynonym "FLJ23741" @default.
- NCIT_C97550 hasExactSynonym "FOXP1 wt Allele" @default.
- NCIT_C97550 hasExactSynonym "Fork Head-Related Protein Like B Gene" @default.
- NCIT_C97550 hasExactSynonym "Forkhead Box P1 wt Allele" @default.
- NCIT_C97550 hasExactSynonym "Glutamine-Rich Factor 1 Gene" @default.
- NCIT_C97550 hasExactSynonym "HSPC215" @default.
- NCIT_C97550 hasExactSynonym "MGC12942" @default.
- NCIT_C97550 hasExactSynonym "MGC88572" @default.
- NCIT_C97550 hasExactSynonym "MGC99551" @default.
- NCIT_C97550 hasExactSynonym "QRF1" @default.
- NCIT_C97550 hasExactSynonym "hFKH1B" @default.
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