Difference between revisions of "YDL160C-A"
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|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Coordinates''' | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Coordinates''' | ||
− | |nowrap| Chr IV: | + | |nowrap| Chr IV:169608..169366 |
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|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Primary SGDID''' || S000028520 | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Primary SGDID''' || S000028520 |
Revision as of 14:05, 3 February 2011
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Systematic name | YDL160C-A |
Gene name | |
Aliases | |
Feature type | ORF, Uncharacterized |
Coordinates | Chr IV:169608..169366 |
Primary SGDID | S000028520 |
Description of YDL160C-A: Putative protein of unknown function; mutant in a srs2 mutant background displays MMS hypersensitivity; ortholog of human MHF2, a component of the Fanconi anemia (FA) complex that is involved in maintaining genome stability[1][2]
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