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Gene: LINC01402 (long intergenic non-protein coding RNA 1402) Homo sapiens
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Symbol: LINC01402
Name: long intergenic non-protein coding RNA 1402
Description: ASSOCIATED WITH autistic disorder
Type: ncrna
RefSeq Status: VALIDATED
Also known as: GS1-421I3.4; TCONS_00017087
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38X120,117,642 - 120,119,700 (-)NCBIGRCh38GRCh38hg38GRCh38
Cytogenetic MapXq24NCBI
CHM1_1X119,162,493 - 119,164,551 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - uncurated

Genomics

miRNA Target Status

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on LINC01402
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 9684915
Created: 2014-12-10
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.