RNA5SP19 (RNA, 5S ribosomal pseudogene 19) - Rat Genome Database

Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models   new Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Gene: RNA5SP19 (RNA, 5S ribosomal pseudogene 19) Homo sapiens
Analyze
Symbol: RNA5SP19
Name: RNA, 5S ribosomal pseudogene 19
RGD ID: 6482075
HGNC Page HGNC:42587
Description:
Type: pseudo (Ensembl: rRNA_pseudogene)
RefSeq Status: INFERRED
Previously known as: RN5S19
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381228,555,793 - 228,555,901 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1228,555,793 - 228,555,901 (+)EnsemblGRCh38hg38GRCh38
GRCh371228,743,494 - 228,743,602 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map1q42.13NCBI
HuRef1199,258,465 - 199,258,573 (+)NCBIHuRef
CHM1_11230,015,761 - 230,015,869 (+)NCBICHM1_1
T2T-CHM13v2.01227,744,287 - 227,744,395 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


References

Genomics

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:223
Count of miRNA genes:218
Interacting mature miRNAs:223
Transcripts:ENST00000365186
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system adipose tissue appendage
High
Medium
Low 7 6 6 13 52 41 9 28 9 49
Below cutoff 34 64 18 6 27 5 180 179 71 1 20 14 2 15 162

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000365186
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1228,555,793 - 228,555,901 (+)Ensembl

Additional Information

Database Acc Id Source(s)
COSMIC RNA5SP19 COSMIC
Ensembl Genes ENSG00000202056 Ensembl, ENTREZGENE
GTEx ENSG00000202056 GTEx
HGNC ID HGNC:42587 ENTREZGENE
Human Proteome Map RNA5SP19 Human Proteome Map
NCBI Gene RN5S19 ENTREZGENE


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2012-08-14 RNA5SP19  RNA, 5S ribosomal pseudogene 19  RN5S19  RNA, 5S ribosomal 19  Symbol and/or name change 5135510 APPROVED