Difference between revisions of "YEL048C"

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'''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='S000130484'>Montpetit B and Conibear E (2009) Identification of the Novel TRAPP Associated Protein Tca17. Traffic 10(6):713-23 {{SGDpaper|S000130484}} PMID 19220810</ref><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='S000130251'>Scrivens PJ, et al. (2009) TRAPPC2L is a Novel, Highly Conserved TRAPP-Interacting Protein. Traffic 10(6):724-36
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'''Description of YEL048C:''' Subunit of TRAPPII, a multimeric GEF involved in intra-Golgi and endosome-to-Golgi transport; promotes association of TRAPPII-specific subunits with the core complex; sedlin related; human Sedlin mutations cause SEDT, a skeletal disorder<ref name='S000144846'>Choi C, et al. (2011) Organization and Assembly of the TRAPPII Complex.LID - 10.1111/j.1600-0854.2011.01181.x [doi] Traffic () {{SGDpaper|S000144846}} PMID 21453443</ref><ref name='S000130484'>Montpetit B and Conibear E (2009) Identification of the Novel TRAPP Associated Protein Tca17. Traffic 10(6):713-23 {{SGDpaper|S000130484}} PMID 19220810</ref><ref name='S000130251'>Scrivens PJ, et al. (2009) TRAPPC2L is a Novel, Highly Conserved TRAPP-Interacting Protein. Traffic 10(6):724-36
 
  {{SGDpaper|S000130251}} PMID 19416478</ref>
 
  {{SGDpaper|S000130251}} PMID 19416478</ref>
 
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Revision as of 14:05, 12 April 2011

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Systematic name YEL048C
Gene name TCA17
Aliases
Feature type ORF, Verified
Coordinates Chr V:65167..64709
Primary SGDID S000000774


Description of YEL048C: Subunit of TRAPPII, a multimeric GEF involved in intra-Golgi and endosome-to-Golgi transport; promotes association of TRAPPII-specific subunits with the core complex; sedlin related; human Sedlin mutations cause SEDT, a skeletal disorder[1][2][3]




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References

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  1. Choi C, et al. (2011) Organization and Assembly of the TRAPPII Complex.LID - 10.1111/j.1600-0854.2011.01181.x [doi] Traffic () SGD PMID 21453443
  2. Montpetit B and Conibear E (2009) Identification of the Novel TRAPP Associated Protein Tca17. Traffic 10(6):713-23 SGD PMID 19220810
  3. Scrivens PJ, et al. (2009) TRAPPC2L is a Novel, Highly Conserved TRAPP-Interacting Protein. Traffic 10(6):724-36 SGD PMID 19416478

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