RNU7-176P (RNA, U7 small nuclear 176 pseudogene) - 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: RNU7-176P (RNA, U7 small nuclear 176 pseudogene) Homo sapiens
Analyze
Symbol: RNU7-176P
Name: RNA, U7 small nuclear 176 pseudogene
RGD ID: 10412496
HGNC Page HGNC:45710
Description:
Type: pseudo (Ensembl: snRNA)
RefSeq Status: INFERRED
Related Functional Gene: RNU7-1  
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38210,815,485 - 10,815,546 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl210,815,485 - 10,815,546 (-)EnsemblGRCh38hg38GRCh38
GRCh37210,955,611 - 10,955,672 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map2p25.1NCBI
CHM1_1210,885,473 - 10,885,534 (-)NCBICHM1_1
T2T-CHM13v2.0210,845,488 - 10,845,549 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


References

Genomics

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:196
Count of miRNA genes:189
Interacting mature miRNAs:195
Transcripts:ENST00000458792
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 adipose tissue appendage
High
Medium 1
Low 9 1 5 3 22 3 8 1 7 6 14 5 1
Below cutoff 1 2 1 1 1 3 2 1 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000458792
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl210,815,485 - 10,815,546 (-)Ensembl

Additional Information

Database Acc Id Source(s)
COSMIC RNU7-176P COSMIC
Ensembl Genes ENSG00000238962 Ensembl, ENTREZGENE
GTEx ENSG00000238962 GTEx
HGNC ID HGNC:45710 ENTREZGENE
Human Proteome Map RNU7-176P Human Proteome Map
NCBI Gene RNU7-176P ENTREZGENE