Characterization of the human gene coding for the swelling-dependent chloride channel ICln at position 11q13.5-14.1 (CLNS1A) and further characterization of the chromosome 6 (CLNS1B) localization
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作者:
Nagl, UO
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机构:Univ Innsbruck, Dept Physiol, A-6020 Innsbruck, Austria
Nagl, UO
Erdel, M
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机构:Univ Innsbruck, Dept Physiol, A-6020 Innsbruck, Austria
Erdel, M
Bergmann, F
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机构:Univ Innsbruck, Dept Physiol, A-6020 Innsbruck, Austria
Bergmann, F
Oehl, B
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机构:Univ Innsbruck, Dept Physiol, A-6020 Innsbruck, Austria
Oehl, B
Scandella, E
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机构:Univ Innsbruck, Dept Physiol, A-6020 Innsbruck, Austria
Scandella, E
Musante, L
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机构:Univ Innsbruck, Dept Physiol, A-6020 Innsbruck, Austria
Musante, L
Galietta, LJV
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机构:Univ Innsbruck, Dept Physiol, A-6020 Innsbruck, Austria
Galietta, LJV
Gschwentner, M
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机构:Univ Innsbruck, Dept Physiol, A-6020 Innsbruck, Austria
Gschwentner, M
Fürst, J
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机构:Univ Innsbruck, Dept Physiol, A-6020 Innsbruck, Austria
Fürst, J
Schmarda, A
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机构:Univ Innsbruck, Dept Physiol, A-6020 Innsbruck, Austria
Schmarda, A
Hofer, S
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机构:Univ Innsbruck, Dept Physiol, A-6020 Innsbruck, Austria
Hofer, S
Utermann, G
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机构:Univ Innsbruck, Dept Physiol, A-6020 Innsbruck, Austria
Utermann, G
Deetjen, P
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机构:Univ Innsbruck, Dept Physiol, A-6020 Innsbruck, Austria
Deetjen, P
Paulmichl, M
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机构:Univ Innsbruck, Dept Physiol, A-6020 Innsbruck, Austria
Paulmichl, M
机构:
[1] Univ Innsbruck, Dept Physiol, A-6020 Innsbruck, Austria
[2] Univ Innsbruck, Dept Med Biol & Human Genet, A-6020 Innsbruck, Austria
[3] Ist Giannina Gaslini, Genet Mol Lab, I-16148 Genoa, Italy
I(Cln);
swelling-dependent chloride channel;
human chromosomal localization;
RVD;
D O I:
10.1016/S0378-1119(98)00002-X
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
Expression cloning revealed a chloride channel (I(Cln)) that we found to be fundamental for the regulatory volume decrease in a variety of cells. The chromosomal localization of the human I(Cln)-gene showed two loci, one at chromosome 11 in position q13.5-q14.1, termed CLNS1A, and a second one at chromosome 6 at position p12.1-q13, termed CLNS1B. In this study, we offer a detailed characterization of the CLNS1A gene and provide the exact position (6p12) and sequence data of CLNS1B, an intronless gene 91.3% homologous to the coding region of CLNS1A. (C) 1998 Elsevier Science B.V.