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Gene: LINC00462 (long intergenic non-protein coding RNA 462) Homo sapiens
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Symbol: LINC00462
Name: long intergenic non-protein coding RNA 462
Description: ASSOCIATED WITH Chromosome 13q Deletion Syndrome; chromosome 13q14 deletion syndrome
Type: ncrna
RefSeq Status: VALIDATED
Also known as: RP11-165D7.4
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl1348,576,974 - 48,578,088 (-)Ensembl
GRCh381348,576,974 - 48,580,901 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371349,151,110 - 49,155,037 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361348,039,735 - 48,062,682 (-)NCBINCBI36hg18NCBI36
Celera1330,196,499 - 30,219,450 (-)NCBI
Cytogenetic Map13q14.2ENTREZGENE
HuRef1329,944,455 - 29,948,382 (-)NCBIHuRef
CHM1_11349,118,662 - 49,122,589 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - uncurated

Genomics

Position Markers
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on LINC00462
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 6484100
Created: 2012-06-05
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.