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

Jutta Gärtner, William Kearns, Carla Rosenberg, Peter Pearson, Neal G. Copeland, Debra J. Gilbert, Nancy A. Jenkins, David Valle

Research output: Contribution to journalArticle

Abstract

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 asigned to human chromosome 1p21-p22 by in situ hybridization and its murine homologue (Pxmp-1) to chromosome 3 by interspecific backcross analysis.

Original languageEnglish (US)
Pages (from-to)412-414
Number of pages3
JournalGenomics
Volume15
Issue number2
DOIs
StatePublished - Feb 1993

ASJC Scopus subject areas

  • Genetics

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    Gärtner, J., Kearns, W., Rosenberg, C., Pearson, P., Copeland, N. G., Gilbert, D. J., Jenkins, N. A., & Valle, D. (1993). Localization of the 70-kda peroxisomal membrane protein to human 1p21-p22 and mouse 3. Genomics, 15(2), 412-414. https://doi.org/10.1006/geno.1993.1076