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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
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


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

CRRD Object Information
CRRD ID: 1602028
Created: 2007-04-27
Species: Homo sapiens
Last Modified: 2019-11-26
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.