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Linkage relationships of the human methylmalonyl CoA mutase to the HLA and D6S4 loci on chromosome 6.

作者信息

Zoghbi H Y, O'Brien W E, Ledley F D

机构信息

Department of Pediatrics, Baylor College of Medicine, Houston, Texas 77030.

出版信息

Genomics. 1988 Nov;3(4):396-8. doi: 10.1016/0888-7543(88)90135-8.

DOI:10.1016/0888-7543(88)90135-8
PMID:2907507
Abstract

The human methylmalonyl CoA mutase (MCM) cDNA has been used to localize the MUT locus on the short arm of chromosome 6 proximal to the glyoxalase locus in 6p deletion cell lines. A HindIII polymorphism identified by the MCM cDNA was used to study linkage relationships of MUT to HLA (A-B-DQ-DR) and D6S4 in the reference CEPH families. The maximum lod score for MUT versus HLA was 3.04 at a recombination fraction of 0.28. The maximum lod score for MUT versus D6S4 was 22.93 at a recombination fraction of 0.01. These data suggest that MUT and D6S4 loci are tightly linked and may be used as one locus in a haplotype form for linkage studies on proximal 6p and diagnostic analysis of pedigrees with mut methylmalonic acidemia.

摘要

相似文献

1
Linkage relationships of the human methylmalonyl CoA mutase to the HLA and D6S4 loci on chromosome 6.
Genomics. 1988 Nov;3(4):396-8. doi: 10.1016/0888-7543(88)90135-8.
2
Mapping of human methylmalonyl CoA mutase (MUT) locus on chromosome 6.人类甲基丙二酰辅酶A变位酶(MUT)基因座在6号染色体上的定位。
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Deletion and linkage mapping of eight markers from the proximal short arm of chromosome 6.
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Mapping of the L-methylmalonyl-CoA mutase gene to mouse chromosome 17.
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Heterogeneous alleles and expression of methylmalonyl CoA mutase in mut methylmalonic acidemia.甲基丙二酸血症中甲基丙二酰辅酶A变位酶的异质等位基因与表达
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J Clin Invest. 1980 Mar;65(3):690-8. doi: 10.1172/JCI109715.

引用本文的文献

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Genomic structure of murine methylmalonyl-CoA mutase: evidence for genetic and epigenetic mechanisms determining enzyme activity.小鼠甲基丙二酰辅酶A变位酶的基因组结构:决定酶活性的遗传和表观遗传机制的证据。
Biochem J. 1993 Dec 15;296 ( Pt 3)(Pt 3):663-70. doi: 10.1042/bj2960663.
2
Heterozygous mutations at the mut locus in fibroblasts with mut0 methylmalonic acidemia identified by polymerase-chain-reaction cDNA cloning.通过聚合酶链反应cDNA克隆鉴定出在患有mut0型甲基丙二酸血症的成纤维细胞中mut位点的杂合突变。
Am J Hum Genet. 1990 Nov;47(5):808-14.
3
TaqI polymorphism at the D6S91 locus.
D6S91基因座处的TaqI多态性
Nucleic Acids Res. 1990 Oct 11;18(19):5923. doi: 10.1093/nar/18.19.5923-a.
4
Autosomal dominant ataxia: genetic evidence for locus heterogeneity from a Cuban founder-effect population.常染色体显性共济失调:来自古巴奠基者效应人群中基因座异质性的遗传学证据。
Am J Hum Genet. 1990 Jun;46(6):1163-77.
5
Heterogeneous alleles and expression of methylmalonyl CoA mutase in mut methylmalonic acidemia.甲基丙二酸血症中甲基丙二酰辅酶A变位酶的异质等位基因与表达
Am J Hum Genet. 1990 Mar;46(3):539-47.
6
Fine mapping of a human chromosome 6 ferritin heavy chain pseudogene: relevance to haemochromatosis.
Hum Genet. 1991 Dec;88(2):175-8. doi: 10.1007/BF00206067.
7
BclI and MspI polymorphisms at the D6S90 locus.D6S90位点的BclI和MspI多态性
Nucleic Acids Res. 1990 Oct 11;18(19):5922. doi: 10.1093/nar/18.19.5922.