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- NCIT_C75728 IAO_0000115 "Human MECP2 wild-type allele is located in the vicinity of Xq28 and is approximately 76 kb in length. This allele, which encodes methyl-CpG-binding protein 2, is involved in transcriptional modulation. Mutations in the gene are associated with a number of congenital neurological diseases." @default.
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- NCIT_C75728 NCIT_P102 "AF158180" @default.
- NCIT_C75728 NCIT_P106 "Gene or Genome" @default.
- NCIT_C75728 NCIT_P108 "MECP2 wt Allele" @default.
- NCIT_C75728 NCIT_P207 "C2697959" @default.
- NCIT_C75728 NCIT_P321 "4204" @default.
- NCIT_C75728 NCIT_P366 "MECP2_wt_Allele" @default.
- NCIT_C75728 NCIT_P98 "Mutations in the MECP2 gene are associated with Angelman syndrome, mental retardation syndromic X-linked type 13, Rett syndrome, susceptibility to X-linked autism 3, and neonatal severe encephalopathy due to MECP2 mutations. A chromosomal duplication, which involves the MECP2 gene, is linked to Lubs type X-linked mental retardation syndrome. (UniProt)" @default.
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- NCIT_C75728 hasExactSynonym "MECP2 wt Allele" @default.
- NCIT_C75728 hasExactSynonym "MECP2" @default.
- NCIT_C75728 hasExactSynonym "Methyl CpG Binding Protein 2 (Rett Syndrome) wt Allele" @default.
- NCIT_C75728 type Class @default.
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- NCIT_C75728 label "MECP2 wt Allele" @default.
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