Difference between revisions of "YPR033C"

From SGD-Wiki
Jump to: navigation, search
(Automated import of articles)
(Automated import of articles)
Line 18: Line 18:
 
|}
 
|}
 
<br>
 
<br>
'''Description of YPR033C:''' Cytoplasmic and mitochondrial histidine tRNA synthetase; efficient mitochondrial localization requires both a presequence and an amino-terminal sequence; mutations in human ortholog HARS2 are associated with Perrault syndrome<ref name='S000042552'>Chiu MI, et al. (1992) HTS1 encodes both the cytoplasmic and mitochondrial histidyl-tRNA synthetase of Saccharomyces cerevisiae: mutations alter the specificity of compartmentation. Genetics 132(4):987-1001 {{SGDpaper|S000042552}} PMID 1459448</ref><ref name='S000043557'>Natsoulis G, et al. (1986) The HTS1 gene encodes both the cytoplasmic and mitochondrial histidine tRNA synthetases of S. cerevisiae. Cell 46(2):235-43 {{SGDpaper|S000043557}} PMID 3521891</ref><ref name='S000144967'>Pierce SB, et al. (2011) Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome. Proc Natl Acad Sci U S A ()
+
'''Description of YPR033C:''' Cytoplasmic and mitochondrial histidine tRNA synthetase; efficient mitochondrial localization requires both a presequence and an amino-terminal sequence; mutations in human ortholog HARS2 are associated with Perrault syndrome<ref name='S000042552'>Chiu MI, et al. (1992) HTS1 encodes both the cytoplasmic and mitochondrial histidyl-tRNA synthetase of Saccharomyces cerevisiae: mutations alter the specificity of compartmentation. Genetics 132(4):987-1001 {{SGDpaper|S000042552}} PMID 1459448</ref><ref name='S000043557'>Natsoulis G, et al. (1986) The HTS1 gene encodes both the cytoplasmic and mitochondrial histidine tRNA synthetases of S. cerevisiae. Cell 46(2):235-43 {{SGDpaper|S000043557}} PMID 3521891</ref><ref name='S000144967'>Pierce SB, et al. (2011) Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome. Proc Natl Acad Sci U S A 108(16):6543-8
 
  {{SGDpaper|S000144967}} PMID 21464306</ref>
 
  {{SGDpaper|S000144967}} PMID 21464306</ref>
 
<br>
 
<br>

Revision as of 13:05, 23 April 2011

Share your knowledge...Edit this entry! <protect>

Systematic name YPR033C
Gene name HTS1
Aliases TSM4572
Feature type ORF, Verified
Coordinates Chr XVI:639019..637379
Primary SGDID S000006237


Description of YPR033C: Cytoplasmic and mitochondrial histidine tRNA synthetase; efficient mitochondrial localization requires both a presequence and an amino-terminal sequence; mutations in human ortholog HARS2 are associated with Perrault syndrome[1][2][3]




</protect>

Community Commentary

About Community Commentary. Please share your knowledge!




<protect>

References

See Help:References on how to add references

  1. Chiu MI, et al. (1992) HTS1 encodes both the cytoplasmic and mitochondrial histidyl-tRNA synthetase of Saccharomyces cerevisiae: mutations alter the specificity of compartmentation. Genetics 132(4):987-1001 SGD PMID 1459448
  2. Natsoulis G, et al. (1986) The HTS1 gene encodes both the cytoplasmic and mitochondrial histidine tRNA synthetases of S. cerevisiae. Cell 46(2):235-43 SGD PMID 3521891
  3. Pierce SB, et al. (2011) Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome. Proc Natl Acad Sci U S A 108(16):6543-8 SGD PMID 21464306

See Help:Categories on how to add the wiki page for this gene to a Category </protect>