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Gene: LINC00992 (long intergenic non-protein coding RNA 992) Homo sapiens
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Symbol: LINC00992
Name: long intergenic non-protein coding RNA 992
Description: ASSOCIATED WITH autistic disorder; INTERACTS WITH dorsomorphin; entinostat; nickel atom
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 Ensembl5117,415,509 - 117,546,298 (+)Ensembl
GRCh385117,415,512 - 117,579,744 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh375116,751,208 - 116,915,439 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 365116,779,104 - 116,940,933 (+)NCBINCBI36hg18NCBI36
Celera5112,700,450 - 112,862,317 (+)NCBI
Cytogenetic Map5q23.1NCBI
HuRef5111,932,410 - 112,097,110 (+)NCBIHuRef
CHM1_15116,183,860 - 116,348,058 (+)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
Promoters
Clinical Variants

Additional Information

External Database Links
 
More on LINC00992
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 7250101
Created: 2013-08-20
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.