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Aliases for RNR2 Gene

Subcategory (RNA class) for RNR2 Gene

non-coding RNA

Quality Score for this RNA gene is

2

Aliases for RNR2 Gene

  • RNA, Ribosomal Cluster 2 2 3
  • RNA, Ribosomal 2 2

External Ids for RNR2 Gene

Summaries for RNR2 Gene

Entrez Gene Summary for RNR2 Gene

  • The genes encoding the rRNA components of the ribosome are organized as tandem rDNA repeating units, designated RNR1 through RNR5, in the p12 region of chromosomes 13, 14, 15, 21 and 22. Each rDNA unit encodes a 45S rRNA which serves as the precursor for an 18S, 5.8S and 28S rRNA. The number of rDNA repeating units varies between individuals and from chromosome to chromosome, although usually 30 to 40 repeats are found on each chromosome. This ribosomal repeating unit located on chromosome 14 is not currently annotated on the reference genome. [provided by RefSeq, Mar 2009]

GeneCards Summary for RNR2 Gene

RNR2 (RNA, Ribosomal Cluster 2) is an RNA Gene, and belongs to the non-coding RNA class. Diseases associated with RNR2 include cyclic vomiting syndrome. Among its related pathways are CFTR translational fidelity (class I mutations).

No data available for UniProtKB/Swiss-Prot , Tocris Summary , Gene Wiki entry , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for RNR2 Gene

Genomics for RNR2 Gene

Genomic Location for RNR2 Gene

Orientation:
Unknown strand

Genomic View for RNR2 Gene

Cytogenetic band:

No data available for RefSeq DNA sequence and Regulatory Elements for RNR2 Gene

Proteins for RNR2 Gene

Post-translational modifications for RNR2 Gene

No Post-translational modifications

No data available for DME Specific Peptides for RNR2 Gene

Domains for RNR2 Gene

Graphical View of Domain Structure for InterPro Entry

No data available for Gene Families , Protein Domains , Suggested Antigen Peptide Sequences and UniProtKB/Swiss-Prot for RNR2 Gene

Function for RNR2 Gene

Molecular function for RNR2 Gene

GENATLAS Biochemistry: RNA,ribosomal cluster 2

No data available for Enzyme Numbers (IUBMB) , Gene Ontology (GO) - Molecular Function , Phenotypes , Animal Models , miRNA , Transcription Factor Targeting and HOMER Transcription for RNR2 Gene

Localization for RNR2 Gene

No data available for Subcellular locations from UniProtKB/Swiss-Prot , Subcellular locations from COMPARTMENTS and Gene Ontology (GO) - Cellular Components for RNR2 Gene

Pathways for RNR2 Gene

genes like me logo Genes that share pathways with RNR2: view

Pathways by source for RNR2 Gene

1 GeneGo (Thomson Reuters) pathway for RNR2 Gene

Interacting Proteins for RNR2 Gene

Gene Ontology (GO) - Biological Process for RNR2 Gene

None

Transcripts for RNR2 Gene

Alternative Splicing Database (ASD) splice patterns (SP) for RNR2 Gene

No ASD Table

Relevant External Links for RNR2 Gene

ECgene alternative splicing isoforms for
RNR2

No data available for mRNA/cDNA for RNR2 Gene

Expression for RNR2 Gene

No Expression Related Data Available

No data available for mRNA expression in normal human tissues , mRNA expression in embryonic tissues and stem cells from LifeMap Discovery , mRNA differential expression in normal tissues , Protein expression and mRNA Expression by UniProt/SwissProt for RNR2 Gene

Orthologs for RNR2 Gene

No data available for Orthologs and Evolution for RNR2 Gene

Paralogs for RNR2 Gene

No data available for Paralogs for RNR2 Gene

Variants for RNR2 Gene

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot , Sequence variations from dbSNP and Humsavar , Structural Variations from Database of Genomic Variants (DGV) and Relevant External Links for RNR2 Gene

Disorders for RNR2 Gene

(1) MalaCards Diseases for RNR2 Gene

Search for RNR2 Gene in MalaCards »

Relevant External Links for RNR2

Genetic Association Database (GAD)
RNR2
Human Genome Epidemiology (HuGE) Navigator
RNR2
genes like me logo Genes that share disorders with RNR2: view

No data available for UniProtKB/Swiss-Prot for RNR2 Gene

Publications for RNR2 Gene

  1. Human rDNA: evolutionary patterns within the genes and tandem arrays derived from multiple chromosomes. (PMID: 11350117) Gonzalez I.L. … Sylvester J.E. (Genomics 2001) 2 3
  2. Are pediatric and adult-onset cyclic vomiting syndrome (CVS) biologically different conditions? Relationship of adult-onset CVS with the migraine and pediatric CVS-associated common mtDNA polymorphisms 16519T and 3010A. (PMID: 19368653) Boles R.G. … McCallum R. (Neurogastroenterol. Motil. 2009) 3 48
  3. Genotyping Parkinson disease-associated mitochondrial polymorphisms. (PMID: 15931342) Jiang Y. … Greenlee A.R. (Clin Med Res 2004) 48
  4. Comprehensive analysis of common mitochondrial DNA variants and colorectal cancer risk. (PMID: 19050702) Webb E. … Houlston R.S. (Br. J. Cancer 2008) 48
  5. Mitochondrial DNA and gastrointestinal motor and sensory functions in health and functional gastrointestinal disorders. (PMID: 19147801) Camilleri M. … Boles R.G. (Am. J. Physiol. Gastrointest. Liver Physiol. 2009) 48

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