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Title: Cohen syndrome is caused by mutations in a novel gene, COH1, encoding a transmembrane protein with a presumed role in vesicle-mediated sorting and intracellular protein transport
Authors: Kolehmainen, Juha ×
Black, Graeme C M
Saarinen, Anne
Chandler, Kate
Clayton-Smith, Jill
Träskelin, Ann-Liz
Perveen, Rahat
Kivitie-Kallio, Satu
Norio, Reijo
Warburg, Mette
Fryns, Jean-Pierre
de la Chapelle, Albert
Lehesjoki, Anna-Elina #
Issue Date: May-2003
Series Title: American Journal of Human Genetics vol:72 issue:6 pages:1359-69
Abstract: Cohen syndrome is an uncommon autosomal recessive disorder whose diagnosis is based on the clinical picture of nonprogressive psychomotor retardation and microcephaly, characteristic facial features, retinal dystrophy, and intermittent neutropenia. We have refined the critical region on chromosome 8q22 by haplotype analysis, and we report the characterization of a novel gene, COH1, that is mutated in patients with Cohen syndrome. The longest transcript (14,093 bp) is widely expressed and is transcribed from 62 exons that span a genomic region of approximately 864 kb. COH1 encodes a putative transmembrane protein of 4,022 amino acids, with a complex domain structure. Homology to the Saccharomyces cerevisiae VPS13 protein suggests a role for COH1 in vesicle-mediated sorting and transport of proteins within the cell.
URI: 
ISSN: 0002-9297
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Clinical Genetics Section (-)
Department of Human Genetics - miscellaneous
× corresponding author
# (joint) last author

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