Partial structure, chromosome localization, and expression of the mouse Icln gene

Kevin Wickman, Michael F. Seldin, Michael R. James, Sandra J. Gendler, David E. Clapham

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

The molecular identities of most volume-regulated ion channel proteins and putative regulatory elements are currently unknown. Recently, a role for a nucleotide-sensitive chloride conductance regulator, ICln, in the function of a ubiquitous volume-regulated chloride channel has been suggested. Here, we report the cloning of a fragment of the mouse Icln gene and identification of probable Icln pseudogenes. The functional Icln gene was mapped independently to human chromosome 11q13.5-q14 and mouse chromosome 7 (50.3 cM). ICln mRNA was shown to be abundantly expressed and evenly distributed in all mouse tissues examined and at four stages of embryonic development, consistent with the proposed role of ICln in the regulation of a ubiquitous chloride channel.

Original languageEnglish (US)
Pages (from-to)402-408
Number of pages7
JournalGenomics
Volume40
Issue number3
DOIs
StatePublished - Mar 15 1997

Bibliographical note

Funding Information:
We thank Dr. Andrew Spicer for helpful comments and technical advice, Dr. Robert Jenkins for providing the human/rodent somatic cell hybrid panels, and Shawn Corey and Dwight Johnson for technical assistance. This work was supported in part by an NIH grant to M.F.S. (HG00734) and by a SCOR grant (IPSO-49184) to S.J.G. and D.E.C.

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