Localization of the 70-kDa peroxisomal membrane pr...[Genomics. 1993]

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1: Genomics. 1993 Feb;15(2):412-4. Links

Localization of the 70-kDa peroxisomal membrane protein to human 1p21-p22 and mouse 3.

Gärtner J, Kearns W, Rosenberg C, Pearson P, Copeland NG, Gilbert DJ, Jenkins NA, Valle D.

Department of Pediatrics, Kennedy Krieger Institute, Johns Hopkins School of Medicine, Baltimore, Maryland 21205.

The 70-kDa peroxisomal membrane protein (PXMP1) is a member of the ATP-binding cassette transporter family. In humans, mutations in this gene may be responsible for a subset of patients with Zellweger syndrome, a lethal inborn error of peroxisome assembly. The PXMP1 gene was assigned to human chromosome 1p21-p22 by in situ hybridization and its murine homologue (Pxmp-1) to chromosome 3 by interspecific backcross analysis.

PMID: 8449508 [PubMed - indexed for MEDLINE]

ReviewThe 70 kDa peroxisomal membrane protein: an ATP-binding cassette transporter protein involved in peroxisome biogenesis. [Semin Cell Biol. 1993]
Genomic organization of the 70-kDa peroxisomal membrane protein gene (PXMP1). [Genomics. 1998]
Mutations in the 70K peroxisomal membrane protein gene in Zellweger syndrome. [Nat Genet. 1992]
Genomic organization and chromosomal localization of the human peroxisomal membrane protein-1-like protein (PXMP1-L) gene encoding a peroxisomal ABC transporter. [FEBS Lett. 1998]
ReviewAdrenoleukodystrophy and other peroxisomal diseases. [Curr Opin Genet Dev. 1994]

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Localization of the 70-kDa peroxisomal membrane protein to human 1p21-p22 and mouse 3.

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