File:CFTRdel4.png

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Description The ΔF508 human genome mutation is characterized by the deletion of three base pairs in the CFTR nucleotide sequence, causing the loss of the amino acid phenylalanine located at position 508.
Source Oak Ridge National Laboratory, Human Genome Project website
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U.S. federal government source.

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Public domain
This work is in the public domain in the United States because it is a work prepared by an officer or employee of the United States Government as part of that person’s official duties under the terms of Title 17, Chapter 1, Section 105 of the US Code. Note: This only applies to original works of the Federal Government and not to the work of any individual U.S. state, territory, commonwealth, county, municipality, or any other subdivision. This template also does not apply to postage stamp designs published by the United States Postal Service since 1978. (See § 313.6(C)(1) of Compendium of U.S. Copyright Office Practices). It also does not apply to certain US coins; see The US Mint Terms of Use.

Original upload log edit

Date/Time Dimensions User Comment
11 July 2008, 21:12:38 275 × 230 (6692 bytes) Twohoos (talk · contribs) {{Information |Description=The [[ΔF508]] [[human genome]] [[mutation]] is characterized by the deletion of three [[base pairs]] in the [[CFTR]] [[nucleotide sequence]], causing the loss of the [[amino acid]] [[phenylalanine]] located at position 508. |So

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Date/TimeThumbnailDimensionsUserComment
current05:39, 28 August 2014Thumbnail for version as of 05:39, 28 August 2014275 × 230 (7 KB)GifTagger (talk | contribs)Bot: Converting file to superior PNG file. (Source: CFTRdel4.gif). This GIF was problematic due to non-greyscale color table.

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