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- NCIT_C75892 IAO_0000115 "Human PITX2 wild-type allele is located within 4q25-q27 and is approximately 25 kb in length. This allele, which encodes pituitary homeobox 2 protein, plays a role in both the modulation of transcription and the regulation of pancreatic development. Mutations in the gene are associated with Rieger syndrome type 1, iridogoniodysgenesis type 2, Peters anomaly, and ring dermoid of cornea." @default.
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- NCIT_C75892 NCIT_P107 "PITX2 wt Allele" @default.
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- NCIT_C75892 hasExactSynonym "ARP1" @default.
- NCIT_C75892 hasExactSynonym "Brx1" @default.
- NCIT_C75892 hasExactSynonym "IDG2" @default.
- NCIT_C75892 hasExactSynonym "IGDS" @default.
- NCIT_C75892 hasExactSynonym "IGDS2" @default.
- NCIT_C75892 hasExactSynonym "IHG2" @default.
- NCIT_C75892 hasExactSynonym "IRID2" @default.
- NCIT_C75892 hasExactSynonym "MGC111022" @default.
- NCIT_C75892 hasExactSynonym "MGC20144" @default.
- NCIT_C75892 hasExactSynonym "Otlx2" @default.
- NCIT_C75892 hasExactSynonym "PITX2 wt Allele" @default.
- NCIT_C75892 hasExactSynonym "PTX2" @default.
- NCIT_C75892 hasExactSynonym "Paired-Like Homeodomain 2 wt Allele" @default.
- NCIT_C75892 hasExactSynonym "Paired-Like Homeodomain Transcription Factor 2 Gene" @default.
- NCIT_C75892 hasExactSynonym "RGS" @default.
- NCIT_C75892 hasExactSynonym "RIEG" @default.
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- NCIT_C75892 type Class @default.
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- NCIT_C75892 label "PITX2 wt Allele" @default.
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