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Gene: DGCR11 (DiGeorge syndrome critical region gene 11) Homo sapiens
Analyze
Symbol: DGCR11
Name: DiGeorge syndrome critical region gene 11
Description: ASSOCIATED WITH autistic disorder; schizophrenia; INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine; 2-hydroxypropanoic acid; bisphenol A
Type: ncrna
RefSeq Status: VALIDATED
Also known as: DGS-D; DiGeorge syndrome critical region gene 11 (non-protein coding)
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl2219,046,162 - 19,048,375 (-)EnsemblGRCh38hg38GRCh38
GRCh382219,046,162 - 19,048,375 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh372219,033,675 - 19,035,888 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362219,033,675 - 19,035,888 (-)NCBINCBI36hg18NCBI36
Build 342217,408,206 - 17,409,463NCBI
Celera222,885,701 - 2,887,914 (-)NCBI
Cytogenetic Map22q11.21NCBI
HuRef222,654,931 - 2,657,144 (-)NCBIHuRef
CHM1_12219,033,290 - 19,035,502 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - curated
References - uncurated

Genomics

Position Markers
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on DGCR11
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1351059
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2020-06-18
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.