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Gene: LINC01653 (long intergenic non-protein coding RNA 1653) Homo sapiens
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Symbol: LINC01653
Name: long intergenic non-protein coding RNA 1653
Description: ASSOCIATED WITH Usher syndrome
Type: ncrna
RefSeq Status: VALIDATED
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381218,043,505 - 218,059,140 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371218,216,847 - 218,232,482 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map1q41NCBI
HuRef1188,885,993 - 188,901,616 (+)NCBIHuRef
CHM1_11219,489,188 - 219,504,824 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - uncurated

Genomics

miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on LINC01653
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 11562706
Created: 2016-11-15
Species: Homo sapiens
Last Modified: 2019-10-16
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.