Difference between revisions of "YBR194W"
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|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Systematic name''' || [http://db.yeastgenome.org/cgi-bin/locus.pl?dbid=S000000398 YBR194W] | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Systematic name''' || [http://db.yeastgenome.org/cgi-bin/locus.pl?dbid=S000000398 YBR194W] | ||
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− | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Gene name''' ||'' | + | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Gene name''' ||''AIM4 '' |
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− | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Aliases''' ||'' '' | + | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Aliases''' ||''SOY1'' |
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|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Feature type''' || ORF, Uncharacterized[[Category:ORF]][[Category:ORF, Uncharacterized]] | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Feature type''' || ORF, Uncharacterized[[Category:ORF]][[Category:ORF, Uncharacterized]] | ||
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− | '''Description of YBR194W:''' Protein proposed to be associated with the nuclear pore complex<ref name='S000056415'>Rout MP, et al. (2000) The yeast nuclear pore complex: composition, architecture, and transport mechanism. J Cell Biol 148(4):635-51 | + | '''Description of YBR194W:''' Protein proposed to be associated with the nuclear pore complex; null mutant displays decreased frequency of mitochondrial genome loss (petite formation) and a severe growth defect in minimal glycerol media<ref name='S000124966'>Hess D, et al. (2008) Integrating computation and experimentation to discover novel mitochondrial biology Science {{SGDpaper|S000124966}} PMID </ref><ref name='S000056415'>Rout MP, et al. (2000) The yeast nuclear pore complex: composition, architecture, and transport mechanism. J Cell Biol 148(4):635-51 |
{{SGDpaper|S000056415}} PMID 10684247</ref> | {{SGDpaper|S000056415}} PMID 10684247</ref> | ||
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Revision as of 13:05, 18 December 2007
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Systematic name | YBR194W |
Gene name | AIM4 |
Aliases | SOY1 |
Feature type | ORF, Uncharacterized |
Coordinates | Chr II:610033..610404 |
Primary SGDID | S000000398 |
Description of YBR194W: Protein proposed to be associated with the nuclear pore complex; null mutant displays decreased frequency of mitochondrial genome loss (petite formation) and a severe growth defect in minimal glycerol media[1][2]
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