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XB-ART-20823
Science 1994 Sep 09;2655178:1585-7.
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Mutations in aquaporin-1 in phenotypically normal humans without functional CHIP water channels.

Preston GM , Smith BL , Zeidel ML , Moulds JJ , Agre P .


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The gene aquaporin-1 encodes channel-forming integral protein (CHIP), a member of a large family of water transporters found throughout nature. Three rare individuals were identified who do not express CHIP-associated Colton blood group antigens and whose red cells exhibit low osmotic water permeabilities. Genomic DNA analyses demonstrated that two individuals were homozygous for different nonsense mutations (exon deletion or frameshift), and the third had a missense mutation encoding a nonfunctioning CHIP molecule. Surprisingly, none of the three suffers any apparent clinical consequence, which raises questions about the physiological importance of CHIP and implies that other mechanisms may compensate for its absence.

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Species referenced: Xenopus
Genes referenced: aqp1