Difference between revisions of "YEL048C"
SGDwikiBot (talk | contribs) (Automated import of articles) |
SGDwikiBot (talk | contribs) (Automated import of articles) |
||
| Line 6: | Line 6: | ||
|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Systematic name''' || [http://db.yeastgenome.org/cgi-bin/locus.pl?dbid=S000000774 YEL048C] | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Systematic name''' || [http://db.yeastgenome.org/cgi-bin/locus.pl?dbid=S000000774 YEL048C] | ||
|- | |- | ||
| − | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Gene name''' ||'' '' | + | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Gene name''' ||''TCA17 '' |
|- | |- | ||
|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Aliases''' ||'' '' | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Aliases''' ||'' '' | ||
| Line 18: | Line 18: | ||
|} | |} | ||
<br> | <br> | ||
| − | '''Description of YEL048C:''' Protein that | + | '''Description of YEL048C:''' Protein that interacts with subunits of the TRAPP complex and may play a role its assembly or stability; mutation is synthetically lethal with gcs1 deletion; Sedlin_N family member; human Sedlin mutations cause the skeletal disorder SEDT<ref name='S000114387'>Robinson M, et al. (2006) The Gcs1 Arf-GAP mediates Snc1,2 v-SNARE retrieval to the Golgi in yeast. Mol Biol Cell 17(4):1845-58 {{SGDpaper|S000114387}} PMID 16452633</ref><ref name='S000130484'>Montpetit B and Conibear E (2009) Identification of the novel TRAPP associated protein Tca17. Traffic {{SGDpaper|S000130484}} PMID 19220810</ref><ref name='S000130251'>Scrivens PJ, et al. (2009) TRAPPC2L is a Novel, Highly Conserved TRAPP-Interacting Protein. Traffic |
{{SGDpaper|S000130251}} PMID 19416478</ref> | {{SGDpaper|S000130251}} PMID 19416478</ref> | ||
<br> | <br> | ||
Revision as of 13:05, 3 June 2009
Share your knowledge...Edit this entry! <protect>
| Systematic name | YEL048C |
| Gene name | TCA17 |
| Aliases | |
| Feature type | ORF, Verified |
| Coordinates | Chr V:65167..64709 |
| Primary SGDID | S000000774 |
Description of YEL048C: Protein that interacts with subunits of the TRAPP complex and may play a role its assembly or stability; mutation is synthetically lethal with gcs1 deletion; Sedlin_N family member; human Sedlin mutations cause the skeletal disorder SEDT[1][2][3]
</protect>
Contents
Community Commentary
About Community Commentary. Please share your knowledge!
<protect>
References
See Help:References on how to add references
- ↑ Robinson M, et al. (2006) The Gcs1 Arf-GAP mediates Snc1,2 v-SNARE retrieval to the Golgi in yeast. Mol Biol Cell 17(4):1845-58 SGD PMID 16452633
- ↑ Montpetit B and Conibear E (2009) Identification of the novel TRAPP associated protein Tca17. Traffic SGD PMID 19220810
- ↑ Scrivens PJ, et al. (2009) TRAPPC2L is a Novel, Highly Conserved TRAPP-Interacting Protein. Traffic SGD PMID 19416478
See Help:Categories on how to add the wiki page for this gene to a Category </protect>
