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Gene: LINC00334 (long intergenic non-protein coding RNA 334) Homo sapiens
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Symbol: LINC00334
Name: long intergenic non-protein coding RNA 334
RGD ID: 1351562
Description: ASSOCIATED WITH autistic disorder; Axenfeld-Rieger syndrome type 3; Neurodevelopmental Disorders; INTERACTS WITH rotenone; silicon dioxide
Type: ncrna
RefSeq Status: VALIDATED
Also known as: C21orf89; NCRNA00334
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl2145,234,308 - 45,264,548 (+)EnsemblGRCh38hg38GRCh38
GRCh382145,234,340 - 45,258,730 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh372146,678,462 - 46,678,563 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362145,502,890 - 45,502,991 (+)NCBINCBI36hg18NCBI36
Build 342145,478,694 - 45,503,073NCBI
Celera2131,786,011 - 31,786,112 (+)NCBI
Cytogenetic Map21q22.3NCBI
HuRef2132,050,444 - 32,050,545 (+)NCBIHuRef
CHM1_12146,215,205 - 46,239,416 (+)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
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on LINC00334
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1351562
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2020-09-16
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.