Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   
Gene: LINC00351 (long intergenic non-protein coding RNA 351) Homo sapiens
Analyze
Symbol: LINC00351
Name: long intergenic non-protein coding RNA 351
Description: ASSOCIATED WITH Chromosome 13q Deletion Syndrome; chromosome 13q14 deletion syndrome
Type: ncrna
RefSeq Status: VALIDATED
Also known as: RP11-76K10.1
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381385,363,603 - 85,544,662 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371385,937,738 - 86,118,797 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map13q31.1NCBI
HuRef1366,647,227 - 66,828,257 (+)NCBIHuRef
CHM1_11385,906,261 - 86,087,327 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - curated
References - uncurated

Genomics

miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on LINC00351
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 6481227
Created: 2012-04-10
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.