"HGNC:9086"^^ . "Human PLP1 wild-type allele is located in the vicinity of Xq22 and is approximately 16 kb in length. This allele, which encodes myelin proteolipid protein, plays a role in the modulation of neuronal development and function. Mutation of the gene is associated with both Pelizaeus-Merzbacher disease and spastic paraplegia type 2.NCI" . "SPG2SYNCI" . _:b699955 . "PLP/DM20SYNCI" . "Proteolipid Protein 1 (Pelizaeus-Merzbacher Disease, Spastic Paraplegia 2, Uncomplicated) wt AlleleSYNCI" . _:b699954 . _:b699954 . _:b699955 . _:b699953 . "C2698697"^^ . "C75898"^^ . "300401"^^ . _:b699954 . "PLP1 wt AllelePTNCI" . _:b699955 . . _:b699953 . "PMDSYNCI" . _:b699953 . "PLP1 wt Allele"^^ . _:b699954 . _:b699955 . . "Gene or Genome"^^ . "PLP1 wt Allele"^^ . "M27110"^^ . _:b699953 . "5354"^^ . "PLP1_wt_Allele"^^ . "PLPSYNCI" . "MMPLSYNCI" .