LOCALIZATION OF THE 70-KDA PEROXISOMAL MEMBRANE-PROTEIN TO HUMAN 1P21-P22 AND MOUSE-3

被引:19
作者
GARTNER, J
KEARNS, W
ROSENBERG, C
PEARSON, P
COPELAND, NG
GILBERT, DJ
JENKINS, NA
VALLE, D
机构
[1] JOHNS HOPKINS UNIV,SCH MED,DEPT PEDIAT,PCTB 802,725 N WOLFE ST,BALTIMORE,MD 21205
[2] NCI,FREDERICK CANC RES & DEV CTR,ABL BASIC RES PROGRAM,FREDERICK,MD 21701
[3] JOHNS HOPKINS UNIV,SCH MED,KENNEDY KRIEGER INST,BALTIMORE,MD 21205
[4] JOHNS HOPKINS UNIV,SCH MED,DEPT MED,BALTIMORE,MD 21205
[5] JOHNS HOPKINS UNIV,SCH MED,HOWARD HUGHES MED INST,BALTIMORE,MD 21205
关键词
D O I
10.1006/geno.1993.1076
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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. © 1993 Academic Press. All rights reserved.
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收藏
页码:412 / 414
页数:3
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