Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   
Gene: SCEL-AS1 (SCEL antisense RNA 1) Homo sapiens
Analyze
Symbol: SCEL-AS1
Name: SCEL antisense RNA 1
Description: ASSOCIATED WITH Chromosome 13q Deletion Syndrome; chromosome 13q14 deletion syndrome; INTERACTS WITH 2-hydroxypropanoic acid; rac-lactic acid
Type: ncrna
RefSeq Status: VALIDATED
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381377,599,755 - 77,606,551 (-)NCBIGRCh38GRCh38hg38GRCh38
Cytogenetic Map13q22.3NCBI
CHM1_11378,141,838 - 78,148,633 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations

Genomics

miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on SCEL-AS1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 9588905
Created: 2014-11-05
Species: Homo sapiens
Last Modified: 2019-11-26
Status: ACTIVE



NHLBI Logo

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