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Gene: LINC01547 (long intergenic non-protein coding RNA 1547) Homo sapiens
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Symbol: LINC01547
Name: long intergenic non-protein coding RNA 1547
Description: ASSOCIATED WITH autistic disorder; INTERACTS WITH all-trans-retinoic acid; amiodarone; antirheumatic drug
Type: ncrna
RefSeq Status: VALIDATED
Also known as: C21orf67; C21orf69; chromosome 21 open reading frame 69; MGC120186; MGC120187; MGC120188; MGC120189; MGC149386; MGC149387; PRED54
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382144,933,284 - 44,939,913 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh372146,353,199 - 46,359,828 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362145,179,076 - 45,184,010 (-)NCBINCBI36hg18NCBI36
Build 342145,179,070 - 45,184,188NCBI
Celera2131,459,702 - 31,466,331 (-)NCBI
Cytogenetic Map21q22.3NCBI
HuRef2131,725,918 - 31,732,547 (-)NCBIHuRef
CHM1_12145,913,795 - 45,920,428 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
References - curated
References - uncurated

Genomics

Position Markers
miRNA Target Status

Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on LINC01547
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1351457
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2019-09-12
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.