Difference between revisions of "YGR136W"
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|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Coordinates''' | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Coordinates''' | ||
| − | |nowrap| Chr VII: | + | |nowrap| Chr VII:762428..763153 |
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|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Primary SGDID''' || S000003368 | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Primary SGDID''' || S000003368 | ||
Revision as of 13:05, 3 February 2011
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| Systematic name | YGR136W |
| Gene name | LSB1 |
| Aliases | |
| Feature type | ORF, Verified |
| Coordinates | Chr VII:762428..763153 |
| Primary SGDID | S000003368 |
Description of YGR136W: Protein containing an N-terminal SH3 domain; binds Las17p, which is a homolog of human Wiskott-Aldrich Syndrome protein involved in actin patch assembly and actin polymerization[1]
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