_:b689774 . "C2697964"^^ . _:b689775 . "Gene or Genome"^^ . "RNF59SYNCI" . "MID1_wt_Allele"^^ . _:b689774 . "MIDINSYNCI" . . "OGS1SYNCI" . "Human MID1 wild-type allele is located in the vicinity of Xp22 and is approximately 388 kb in length. This allele, which encodes midline-1 protein, plays a role in the modulation of microtubule organization. Mutations in this gene may be associated with the X-linked form of Opitz syndrome.NCI" . "FXYSYNCI" . "Midline 1 (Opitz/BBB Syndrome) wt AlleleSYNCI" . "300552"^^ . "OSSYNCI" . "4281"^^ . "Y13667"^^ . "OSXSYNCI" . "MID1 wt Allele"^^ . _:b689775 . "ZNFXYSYNCI" . "C75731"^^ . "BBBG1SYNCI" . _:b689774 . _:b689774 . "MID1 wt AllelePTNCI" . "HGNC:7095"^^ . . "TRIM18SYNCI" . "XPRFSYNCI" . "MID1 wt Allele"^^ . "GBBB1SYNCI" . _:b689775 . _:b689775 .