Literature DB >> 7896277

SCNN1, an epithelial cell sodium channel gene in the conserved linkage group on mouse chromosome 6 and human chromosome 12.

M H Meisler1, L L Barrow, C M Canessa, B C Rossier.   

Abstract

SCNN1, 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).

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 7896277     DOI: 10.1006/geno.1994.1599

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  2 in total

1.  Megencephaly: a new mouse mutation on chromosome 6 that causes hypertrophy of the brain.

Authors:  L R Donahue; S A Cook; K R Johnson; R T Bronson; M T Davisson
Journal:  Mamm Genome       Date:  1996-12       Impact factor: 2.957

2.  Collecting duct-specific gene inactivation of alphaENaC in the mouse kidney does not impair sodium and potassium balance.

Authors:  Isabelle Rubera; Johannes Loffing; Lawrence G Palmer; Gustavo Frindt; Nicole Fowler-Jaeger; Daniel Sauter; Tom Carroll; Andrew McMahon; Edith Hummler; Bernard C Rossier
Journal:  J Clin Invest       Date:  2003-08       Impact factor: 14.808

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.