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Gene: LINC00628 (long intergenic non-protein coding RNA 628) Homo sapiens
Analyze
Symbol: LINC00628
Name: long intergenic non-protein coding RNA 628
Description: ASSOCIATED WITH autistic disorder; INTERACTS WITH aflatoxin B1
Type: ncrna
RefSeq Status: VALIDATED
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381204,368,430 - 204,369,719 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371204,337,558 - 204,338,847 (-)NCBIGRCh37GRCh37hg19GRCh37
Celera1177,472,992 - 177,474,281 (-)NCBI
Cytogenetic Map1q32.1NCBI
HuRef1175,502,505 - 175,503,794 (-)NCBIHuRef
CHM1_11205,761,427 - 205,762,716 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - uncurated

Genomics


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on LINC00628
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 6784183
Created: 2012-07-31
Species: Homo sapiens
Last Modified: 2019-10-16
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.