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Gene: DIAPH3-AS2 (DIAPH3 antisense RNA 2) Homo sapiens
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Symbol: DIAPH3-AS2
Name: DIAPH3 antisense RNA 2
Description: ASSOCIATED WITH Chromosome 13q Deletion Syndrome; chromosome 13q14 deletion syndrome
Type: ncrna
RefSeq Status: VALIDATED
Also known as: DIPAH3-AS2; RP11-430I3.2
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl1360,144,648 - 60,153,678 (+)Ensembl
GRCh381360,144,698 - 60,153,505 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371360,718,832 - 60,727,713 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map13q21.2NCBI
HuRef1341,409,001 - 41,417,839 (+)NCBIHuRef
CHM1_11360,686,553 - 60,695,357 (+)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
Nomenclature History
 
More on DIAPH3-AS2
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 6481152
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.