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Gene: LINC01446 (long intergenic non-protein coding RNA 1446) Homo sapiens
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Symbol: LINC01446
Name: long intergenic non-protein coding RNA 1446
Description: ASSOCIATED WITH autistic disorder
Type: ncrna
RefSeq Status: VALIDATED
Also known as: GS1-179L18.1
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl753,655,508 - 53,811,952 (-)EnsemblGRCh38hg38GRCh38
GRCh38753,655,509 - 53,811,931 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37753,723,202 - 53,879,624 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36753,801,332 - 53,847,112 (-)NCBINCBI36hg18NCBI36
Celera753,783,722 - 53,940,133 (-)NCBI
Cytogenetic Map7p12.1NCBI
HuRef753,572,306 - 53,729,239 (-)NCBIHuRef
CHM1_1753,725,882 - 53,882,311 (-)NCBICHM1_1
CRA_TCAGchr7v2753,728,628 - 53,885,030 (-)NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - curated

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on LINC01446
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1602028
Created: 2007-04-27
Species: Homo sapiens
Last Modified: 2020-03-24
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.