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An integrated genetic map of the pearl locus of mouse chromosome 13.

作者信息

Seymour A B, Yanak B L, O'Brien E P, Rusiniak M E, Novak E K, Pinto L H, Swank R T, Gorin M B

机构信息

Department of Human Genetics, University of Pittsburgh, Pennsylvania 15213, USA.

出版信息

Genome Res. 1996 Jun;6(6):538-44. doi: 10.1101/gr.6.6.538.

DOI:10.1101/gr.6.6.538
PMID:8828042
Abstract

We have used a Mus domesticus/spretus congenic animal and two interspecific backcross panels to map genetically 30 sequence-tagged sites (STSs) and 13 genes to the vicinity of the pearl locus on mouse chromosome 13. The STSs defining the mapped region are from D13Mit9 to D13Mit37, spanning 10.6 cM. Genes mapped to this region include Versican (Cspg2), GTPase activating protein (Rasa), dihydrofolate reductase (Dhfr), arylsulfatase (As-1), thrombin receptor (Cf2r), hexosaminidase b(Hexb), 3-hydroxy-3-methylglutaryl coenzyme A reductase (Hmgcr), microtubule associated protein 5/1b (Mtap5), phosphodiesterase (Pde), phosphatidylinositol 3' kinase (Pik3rl), rat integrin a1-subunit (Itga1), collagen receptor a2-subunit (Itga2), and 5-hydroxytryptamine 1a receptor (Htr1a). This high resolution genetic map of the pearl region of chromosome 13 establishes the order of multiple markers, including genes whose human homologs are located within a limited region of human chromosome 5, with respect to the phenotypic anchor marker pearl.

摘要

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引用本文的文献

1
rim2 (recombination-induced mutation 2) is a new allele of pearl and a mouse model of human Hermansky-Pudlak syndrome (HPS): genetic and physical mapping.rim2(重组诱导突变2)是珍珠色基因的一个新等位基因,也是人类赫尔曼斯基-普德拉克综合征(HPS)的小鼠模型:遗传和物理图谱分析。
Mamm Genome. 1998 Jan;9(1):2-7. doi: 10.1007/s003359900670.