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Gene: DGCR9 (DiGeorge syndrome critical region gene 9) Homo sapiens
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Symbol: DGCR9
Name: DiGeorge syndrome critical region gene 9
Description: ASSOCIATED WITH autistic disorder; schizophrenia; INTERACTS WITH aflatoxin B1; cisplatin; valproic acid
Type: ncrna
RefSeq Status: VALIDATED
Also known as: DGS-A; DiGeorge syndrome critical region gene 9 (non-protein coding)
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382219,017,834 - 19,020,248 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh372219,005,347 - 19,007,761 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 362219,005,347 - 19,007,761 (+)NCBINCBI36hg18NCBI36
Build 342217,380,002 - 17,382,311NCBI
Celera222,857,370 - 2,859,784 (+)NCBI
Cytogenetic Map22q11.21NCBI
HuRef222,626,432 - 2,628,846 (+)NCBIHuRef
CHM1_12219,005,005 - 19,007,419 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - uncurated

Genomics

Position Markers
miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on DGCR9
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1343276
Created: 2005-03-08
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.