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SCNN1, an Epithelial Cell Sodium Channel Gene in the Conserved Linkage Group on Mouse Chromosome 6 and Human Chromosome 12
dc.contributor.authorMeisler, Miriam H.en_US
dc.contributor.authorBarrow, Lon L.en_US
dc.contributor.authorCanessa, Cecilia M.en_US
dc.contributor.authorRossier, Bernard C.en_US
dc.date.accessioned2006-04-10T17:46:23Z
dc.date.available2006-04-10T17:46:23Z
dc.date.issued1994-11-01en_US
dc.identifier.citationMeisler, Miriam H., Barrow, Lon L., Canessa, Cecilia M., Rossier, Bernard C. (1994/11/01)."SCNN1, an Epithelial Cell Sodium Channel Gene in the Conserved Linkage Group on Mouse Chromosome 6 and Human Chromosome 12." Genomics 24(1): 185-186. <http://hdl.handle.net/2027.42/31204>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WG1-45PMRX4-CP/2/c9f60f29afabc8a721a4916e1839068ben_US
dc.identifier.urihttps://hdl.handle.net/2027.42/31204
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=7896277&dopt=citationen_US
dc.description.abstractSCNN1, a gene encoding a nonvoltage-gated sodium channel, was detected using a rat colon cDNA probe with homology to Caenorhabditis elegans degenerin genes. Human SCNN1 was assigned to chromosome 12 using the NIGMS hybrid mapping panel 2. Mouse SCNN1 was mapped to a conserved linkage group on distal chromosome 6. The observed order of mouse genes was centromere-Raf1-(2.1 +/- 2.1)-Scnn1, Vwf -(1.9 +/- 1.9)-Ntf3, with 0/101 recombinants between Scnn1 and Vwf. No rearrangements of genomic DNA were detected in the linked mouse mutations deaf waddler (dfw) and opisthotonus (opt).en_US
dc.format.extent141612 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleSCNN1, an Epithelial Cell Sodium Channel Gene in the Conserved Linkage Group on Mouse Chromosome 6 and Human Chromosome 12en_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan, Ann Arbor, Michigan 48109-0618en_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan, Ann Arbor, Michigan 48109-0618en_US
dc.contributor.affiliationotherInstitut de Pharmacologie et de Toxicologie de l'Universitie, Rue du Bugnon 27, CH-1005 Lausanne, Switzerlanden_US
dc.contributor.affiliationotherInstitut de Pharmacologie et de Toxicologie de l'Universitie, Rue du Bugnon 27, CH-1005 Lausanne, Switzerlanden_US
dc.identifier.pmid7896277en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/31204/1/0000106.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1006/geno.1994.1599en_US
dc.identifier.sourceGenomicsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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