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Gene: LINC00383 (long intergenic non-protein coding RNA 383) Homo sapiens
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Symbol: LINC00383
Name: long intergenic non-protein coding RNA 383
Description: ASSOCIATED WITH Chromosome 13q Deletion Syndrome; chromosome 13q14 deletion syndrome
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LINC00401
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381369,222,346 - 69,322,101 (+)NCBIGRCh38GRCh38hg38GRCh38
Cytogenetic Map13q21.33NCBI
CHM1_11369,764,046 - 69,863,720 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - curated

Genomics

miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on LINC00383
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 8699002
Created: 2014-08-13
Species: Homo sapiens
Last Modified: 2019-11-26
Status: ACTIVE



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