RNH202/YDR279W Summary Help

RNH202 BASIC INFORMATION

Standard Name RNH202 1
Systematic Name YDR279W
Feature Type ORF, Verified
Description Ribonuclease H2 subunit, required for RNase H2 activity; related to human AGS2 that causes Aicardi-Goutieres syndrome (1, 2)
Name Description RNase H 1
Gene Product Alias Rnh2B
GO Annotations All RNH202 GO evidence and references
    View Computational GO annotations for RNH202
Molecular Function
Manually curated
Biological Process
Manually curated
Cellular Component
Manually curated
High-throughput
Mutant Phenotype All RNH202 Phenotype details and references
Large-scale survey
null
Interactions RNH202 All interactions details and references
  View additional details at BioGRID
61 total interaction(s) for 40 unique genes/features.
Physical Interactions
  • Affinity Capture-MS: 5
  • Biochemical Activity: 1
  • Two-hybrid: 1

Genetic Interactions
  • Dosage Lethality: 1
  • Negative Genetic: 38
  • Phenotypic Suppression: 1
  • Positive Genetic: 2
  • Synthetic Growth Defect: 5
  • Synthetic Lethality: 7

Sequence Information
ChrIV:1019365 to 1020417 | ORF Map | GBrowse
Gbrowse
Last Update Coordinates: 2008-06-05 | Sequence: 1996-07-31
Subfeature details
Relative
Coordinates
Chromosomal
Coordinates
Most Recent Updates
Coordinates Sequence
CDS 1..1053 1019365..1020417 2008-06-05 1996-07-31
Post-translational Modifications PhosphoGRID | PhosphoPep Database
External Links All Associated Seq | Entrez Gene | Entrez RefSeq Protein | MIPS | UniProtKB
Primary SGDIDS000002687

RNH202 RESOURCES

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SGD ORF map
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  • Functional Analysis

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Expression Summary histogram

REFERENCES CITED ON THIS PAGE [View Complete Literature Guide for RNH202]

1) Jeong HS, et al.  (2004) RNase H2 of Saccharomyces cerevisiae is a complex of three proteins. Nucleic Acids Res 32(2):407-14
2) Crow YJ, et al.  (2006) Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutieres syndrome and mimic congenital viral brain infection. Nat Genet 38(8):910-6