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Gene: LINC00929 (long intergenic non-protein coding RNA 929) Homo sapiens
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Symbol: LINC00929
Name: long intergenic non-protein coding RNA 929
Description: ASSOCIATED WITH autistic disorder; schizophrenia
Type: ncrna
RefSeq Status: VALIDATED
Also known as: RP11-1084I9.3
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl1526,115,726 - 26,134,001 (+)EnsemblGRCh38hg38GRCh38
GRCh381526,115,813 - 26,133,037 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371526,360,960 - 26,378,184 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map15q12NCBI
HuRef154,490,041 - 4,507,271 (+)NCBIHuRef
CHM1_11526,310,763 - 26,327,997 (+)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 LINC00929
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 7244679
Created: 2013-06-04
Species: Homo sapiens
Last Modified: 2020-03-24
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.