Difference between revisions of "YJL059W"
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| − | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Systematic name''' || [http:// | + | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Systematic name''' || [http://www.yeastgenome.org/cgi-bin/locus.pl?dbid=S000003595 YJL059W] |
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|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Gene name''' ||''YHC3 '' | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Gene name''' ||''YHC3 '' | ||
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|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Coordinates''' | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Coordinates''' | ||
| − | |nowrap| Chr X: | + | |nowrap| Chr X:324964..326190 |
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|valign="top" nowrap bgcolor="{{SGDblue}}"| '''Primary SGDID''' || S000003595 | |valign="top" nowrap bgcolor="{{SGDblue}}"| '''Primary SGDID''' || S000003595 | ||
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| − | '''Description of YJL059W:''' Vacuolar membrane protein involved in the ATP-dependent transport of arginine into the vacuole and possibly in balancing ion homeostasis; homolog of human CLN3 involved in Batten disease (juvenile onset neuronal ceroid lipofuscinosis)<ref name=' | + | '''Description of YJL059W:''' Vacuolar membrane protein involved in the ATP-dependent transport of arginine into the vacuole and possibly in balancing ion homeostasis; homolog of human CLN3 involved in Batten disease (juvenile onset neuronal ceroid lipofuscinosis)<ref name='S000046600'>Croopnick JB, et al. (1998) The subcellular location of the yeast Saccharomyces cerevisiae homologue of the protein defective in the juvenile form of Batten disease. Biochem Biophys Res Commun 250(2):335-41 {{SGDpaper|S000046600}} PMID 9753630</ref><ref name='S000075209'>Kim Y, et al. (2003) A role in vacuolar arginine transport for yeast Btn1p and for human CLN3, the protein defective in Batten disease. Proc Natl Acad Sci U S A 100(26):15458-62 {{SGDpaper|S000075209}} PMID 14660799</ref><ref name='S000080825'>Kim Y, et al. (2005) Interaction among Btn1p, Btn2p, and Ist2p reveals potential interplay among the vacuole, amino acid levels, and ion homeostasis in the yeast Saccharomyces cerevisiae. Eukaryot Cell 4(2):281-8 {{SGDpaper|S000080825}} PMID 15701790</ref><ref name='S000043112'>Mitchison HM, et al. (1997) Structure of the CLN3 gene and predicted structure, location and function of CLN3 protein. Neuropediatrics 28(1):12-4 {{SGDpaper|S000043112}} PMID 9151311</ref><ref name='S000048793'>Pearce DA and Sherman F (1997) BTN1, a yeast gene corresponding to the human gene responsible for Batten's disease, is not essential for viability, mitochondrial function, or degradation of mitochondrial ATP synthase. Yeast 13(8):691-7 |
| − | {{SGDpaper| | + | {{SGDpaper|S000048793}} PMID 9219333</ref> |
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Latest revision as of 06:45, 23 January 2012
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| Systematic name | YJL059W |
| Gene name | YHC3 |
| Aliases | BTN1 |
| Feature type | ORF, Verified |
| Coordinates | Chr X:324964..326190 |
| Primary SGDID | S000003595 |
Description of YJL059W: Vacuolar membrane protein involved in the ATP-dependent transport of arginine into the vacuole and possibly in balancing ion homeostasis; homolog of human CLN3 involved in Batten disease (juvenile onset neuronal ceroid lipofuscinosis)[1][2][3][4][5]
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References
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- ↑ Croopnick JB, et al. (1998) The subcellular location of the yeast Saccharomyces cerevisiae homologue of the protein defective in the juvenile form of Batten disease. Biochem Biophys Res Commun 250(2):335-41 SGD PMID 9753630
- ↑ Kim Y, et al. (2003) A role in vacuolar arginine transport for yeast Btn1p and for human CLN3, the protein defective in Batten disease. Proc Natl Acad Sci U S A 100(26):15458-62 SGD PMID 14660799
- ↑ Kim Y, et al. (2005) Interaction among Btn1p, Btn2p, and Ist2p reveals potential interplay among the vacuole, amino acid levels, and ion homeostasis in the yeast Saccharomyces cerevisiae. Eukaryot Cell 4(2):281-8 SGD PMID 15701790
- ↑ Mitchison HM, et al. (1997) Structure of the CLN3 gene and predicted structure, location and function of CLN3 protein. Neuropediatrics 28(1):12-4 SGD PMID 9151311
- ↑ Pearce DA and Sherman F (1997) BTN1, a yeast gene corresponding to the human gene responsible for Batten's disease, is not essential for viability, mitochondrial function, or degradation of mitochondrial ATP synthase. Yeast 13(8):691-7 SGD PMID 9219333
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