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Gene: LINC00358 (long intergenic non-protein coding RNA 358) Homo sapiens
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Symbol: LINC00358
Name: long intergenic non-protein coding RNA 358
Description: ASSOCIATED WITH Chromosome 13q Deletion Syndrome; chromosome 13q14 deletion syndrome
Type: ncrna
RefSeq Status: VALIDATED
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl1361,997,136 - 62,029,572 (-)Ensembl
GRCh381362,003,525 - 62,029,548 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371362,577,658 - 62,603,681 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map13q21.31NCBI
HuRef1343,270,835 - 43,297,212 (-)NCBIHuRef
CHM1_11362,545,215 - 62,571,218 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - uncurated

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on LINC00358
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 6481230
Created: 2012-04-10
Species: Homo sapiens
Last Modified: 2019-12-25
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.