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Gene: DIAPH3-AS1 (DIAPH3 antisense RNA 1) Homo sapiens
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Symbol: DIAPH3-AS1
Name: DIAPH3 antisense RNA 1
Description: ASSOCIATED WITH Chromosome 13q Deletion Syndrome; chromosome 13q14 deletion syndrome; INTERACTS WITH leflunomide
Type: ncrna
RefSeq Status: VALIDATED
Also known as: RP11-442F12.2
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381360,012,718 - 60,044,357 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371360,586,885 - 60,618,491 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map13q21.2NCBI
HuRef1341,277,263 - 41,308,678 (+)NCBIHuRef
CHM1_11360,554,449 - 60,586,195 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - uncurated

Genomics

miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on DIAPH3-AS1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 6481150
Created: 2012-04-10
Species: Homo sapiens
Last Modified: 2019-11-26
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.