Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   
Gene: HNRNPUL2-BSCL2 (HNRNPUL2-BSCL2 readthrough (NMD candidate)) Homo sapiens
Analyze
Symbol: HNRNPUL2-BSCL2
Name: HNRNPUL2-BSCL2 readthrough (NMD candidate)
RGD ID: 7375939
Description: This locus represents naturally occurring read-through transcription between the neighboring HNRNPUL2 (heterogeneous nuclear ribonucleoprotein U-like 2) and BSCL2 (Berardinelli-Seip congenital lipodystrophy 2 (seipin)) genes on chromosome 11. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is unlikely to produce a protein product. [provided by RefSeq, Mar 2011]
Type: ncrna
RefSeq Status: VALIDATED
Orthologs:
No known orthologs. homologs ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1162,690,275 - 62,727,384 (-)EnsemblGRCh38hg38GRCh38
GRCh381162,690,262 - 62,727,384 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371162,457,734 - 62,494,856 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map11q12.3NCBI
HuRef1158,786,515 - 58,823,578 (-)NCBIHuRef
CHM1_11162,340,845 - 62,377,918 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


References - curated
References - uncurated

Genomics

Position Markers
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on HNRNPUL2-BSCL2
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 7375939
Created: 2013-10-22
Species: Homo sapiens
Last Modified: 2020-09-16
Status: ACTIVE



NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.