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- NCIT_C73462 IAO_0000115 "Human CNTNAP2 wild-type allele is located within 7q35-q36 and is approximately 2305 kb in length. This allele, which encodes contactin associated protein-like 2, may play a role in axonal organization. Mutations in this gene are associated with cortical dysplasia-focal epilepsy syndrome and may be involved in autism and the DFNB13 form of nonsyndromic deafness." @default.
- NCIT_C73462 NCIT_NHC0 "C73462" @default.
- NCIT_C73462 NCIT_P100 "604569" @default.
- NCIT_C73462 NCIT_P102 "AF193613" @default.
- NCIT_C73462 NCIT_P106 "Gene or Genome" @default.
- NCIT_C73462 NCIT_P108 "CNTNAP2 wt Allele" @default.
- NCIT_C73462 NCIT_P207 "C2347280" @default.
- NCIT_C73462 NCIT_P321 "26047" @default.
- NCIT_C73462 NCIT_P366 "CNTNAP2_wt_Allele" @default.
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- NCIT_C73462 NCIT_R41 NCIT_C25796 @default.
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- NCIT_C73462 hasExactSynonym "AUTS15" @default.
- NCIT_C73462 hasExactSynonym "CASPR2" @default.
- NCIT_C73462 hasExactSynonym "CDFE" @default.
- NCIT_C73462 hasExactSynonym "CNTNAP2 wt Allele" @default.
- NCIT_C73462 hasExactSynonym "Contactin Associated Protein-Like 2 wt Allele" @default.
- NCIT_C73462 hasExactSynonym "DKFZp781D1846" @default.
- NCIT_C73462 hasExactSynonym "Homolog of Drosophila Neurexin IV Gene" @default.
- NCIT_C73462 hasExactSynonym "KIAA0868" @default.
- NCIT_C73462 hasExactSynonym "NRXN4" @default.
- NCIT_C73462 hasExactSynonym "Neurexin IV, Drosophila, Homolog of Gene" @default.
- NCIT_C73462 hasExactSynonym "PTHSL1" @default.
- NCIT_C73462 type Class @default.
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- NCIT_C73462 label "CNTNAP2 wt Allele" @default.
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