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Gene: LINC00891 (long intergenic non-protein coding RNA 891) Homo sapiens
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Symbol: LINC00891
Name: long intergenic non-protein coding RNA 891
Description: ASSOCIATED WITH autistic disorder
Type: ncrna
RefSeq Status: VALIDATED
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38X71,697,196 - 71,703,406 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X70,917,046 - 70,923,256 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36X70,837,379 - 70,839,571 (+)NCBINCBI36hg18NCBI36
CeleraX71,269,311 - 71,275,543 (+)NCBI
Cytogenetic MapXq13.1NCBI
HuRefX64,750,952 - 64,757,185 (-)NCBIHuRef
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - uncurated

Genomics


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on LINC00891
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 7254441
Created: 2013-08-20
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.