YPL241C
Revision as of 06:21, 26 February 2009 by SGDwikiBot (talk | contribs) (Automated import of articles)
Share your knowledge...Edit this entry! <protect>
Systematic name | YPL241C |
Gene name | CIN2 |
Aliases | |
Feature type | ORF, Verified |
Coordinates | Chr XVI:96258..95372 |
Primary SGDID | S000006162 |
Description of YPL241C: GTPase-activating protein (GAP) for Cin4p; tubulin folding factor C involved in beta-tubulin (Tub2p) folding; mutants display increased chromosome loss and benomyl sensitivity; deletion complemented by human GAP, retinitis pigmentosa 2[1][2][3][4]
</protect>
Contents
Community Commentary
About Community Commentary. Please share your knowledge!
<protect>
References
See Help:References on how to add references
- ↑ Veltel S, et al. (2008) The retinitis pigmentosa 2 gene product is a GTPase-activating protein for Arf-like 3. Nat Struct Mol Biol 15(4):373-80 SGD PMID 18376416
- ↑ Tian G, et al. (1996) Pathway leading to correctly folded beta-tubulin. Cell 86(2):287-96 SGD PMID 8706133
- ↑ Stearns T, et al. (1990) Yeast mutants sensitive to antimicrotubule drugs define three genes that affect microtubule function. Genetics 124(2):251-62 SGD PMID 2407611
- ↑ Hoyt MA, et al. (1990) Chromosome instability mutants of Saccharomyces cerevisiae that are defective in microtubule-mediated processes. Mol Cell Biol 10(1):223-34 SGD PMID 2403635
See Help:Categories on how to add the wiki page for this gene to a Category </protect>