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Cloning of the gene for ocular albinism type 1 from the distal short arm of the X chromosome.
Bassi, M T; Schiaffino, M V; Renieri, A; De Nigris, F; Galli, L; Bruttini, M; Gebbia, M; Bergen, A A; Lewis, R A; Ballabio, A.
Affiliation
  • Bassi MT; Department of Molecular Biology, University of Siena, Italy.
Nat Genet ; 10(1): 13-9, 1995 May.
Article in En | MEDLINE | ID: mdl-7647783
Ocular albinism type 1 (OA1) is an X-linked disorder characterized by severe impairment of visual acuity, retinal hypopigmentation and the presence of macromelanosomes. We isolated a novel transcript from the OA1 critical region in Xp22.3-22.2 which is expressed at high levels in RNA samples from retina, including the retinal pigment epithelium, and from melanoma. This gene encodes a protein of 424 amino acids displaying several putative transmembrane domains and sharing no similarities with previously identified molecules. Five intragenic deletions and a 2 bp insertion resulting in a premature stop codon were identified from DNA analysis of patients with OA1, indicating that we have identified the OA1 gene.
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Collection: 01-internacional Database: MEDLINE Main subject: X Chromosome / Membrane Glycoproteins / Albinism, Ocular / Eye Proteins / Membrane Proteins Limits: Female / Humans / Male Language: En Journal: Nat Genet Journal subject: GENETICA MEDICA Year: 1995 Document type: Article Affiliation country: Italy Country of publication: United States
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Collection: 01-internacional Database: MEDLINE Main subject: X Chromosome / Membrane Glycoproteins / Albinism, Ocular / Eye Proteins / Membrane Proteins Limits: Female / Humans / Male Language: En Journal: Nat Genet Journal subject: GENETICA MEDICA Year: 1995 Document type: Article Affiliation country: Italy Country of publication: United States