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Gene: LINC00378 (long intergenic non-protein coding RNA 378) Homo sapiens
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Symbol: LINC00378
Name: long intergenic non-protein coding RNA 378
Description: ASSOCIATED WITH Chromosome 13q Deletion Syndrome; chromosome 13q14 deletion syndrome
Type: ncrna
RefSeq Status: VALIDATED
Also known as: RP11-521H3.1
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl1360,618,991 - 61,176,758 (+)Ensembl
GRCh381360,672,955 - 60,695,806 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371361,251,966 - 61,264,998 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map13q21.2NCBI
HuRef1341,943,686 - 41,956,744 (+)NCBIHuRef
CHM1_11361,214,748 - 61,237,605 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on LINC00378
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 6481241
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.