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Gene: LINC00269 (long intergenic non-protein coding RNA 269) Homo sapiens
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Symbol: LINC00269
Name: long intergenic non-protein coding RNA 269
Description: ASSOCIATED WITH autistic disorder; INTERACTS WITH benzo[e]pyrene; methapyrilene; rotenone
Type: ncrna
RefSeq Status: VALIDATED
Also known as: CXorf62; FLJ33610; NCRNA00269; RP13-153N15.1
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 EnsemblX69,179,557 - 69,209,924 (+)Ensembl
GRCh38X69,179,557 - 69,209,924 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X68,399,400 - 68,429,767 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic MapXq13.1NCBI
HuRefX62,223,305 - 62,254,295 (+)NCBIHuRef
CHM1_1X68,292,809 - 68,323,183 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - uncurated

Genomics

Position Markers
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on LINC00269
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1626579
Created: 2007-08-10
Species: Homo sapiens
Last Modified: 2019-12-25
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.