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Gene: LINC00163 (long intergenic non-protein coding RNA 163) Homo sapiens
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Symbol: LINC00163
Name: long intergenic non-protein coding RNA 163
Description: ASSOCIATED WITH autistic disorder; Axenfeld-Rieger syndrome type 3; Neurodevelopmental Disorders
Type: ncrna
RefSeq Status: VALIDATED
Also known as: C21orf134; NCRNA00163; NLC1-A; NLC1A
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382144,989,864 - 44,994,086 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh372146,409,779 - 46,414,001 (-)NCBIGRCh37GRCh37hg19GRCh37
Celera2131,516,360 - 31,520,620 (-)NCBI
Cytogenetic Map21q22.3NCBI
HuRef2131,782,561 - 31,787,745 (-)NCBIHuRef
CHM1_12145,969,426 - 45,974,840 (-)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
Nomenclature History
 
More on LINC00163
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1641971
Created: 2007-08-24
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.