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Gene: LINC01123 (long intergenic non-protein coding RNA 1123) Homo sapiens
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Symbol: LINC01123
Name: long intergenic non-protein coding RNA 1123
Description: ASSOCIATED WITH autism spectrum disorder; INTERACTS WITH triclosan
Type: ncrna
RefSeq Status: VALIDATED
Also known as: AC013268.5
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl2109,987,063 - 109,996,140 (+)Ensembl
GRCh382109,986,980 - 109,995,281 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh372110,744,557 - 110,752,858 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map2q13NCBI
CHM1_12110,750,181 - 110,757,073 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
 
More on LINC01123
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 7383653
Created: 2013-10-22
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.