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Gene: CECR3 (cat eye syndrome chromosome region, candidate 3) Homo sapiens
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Symbol: CECR3
Name: cat eye syndrome chromosome region, candidate 3
Description: ASSOCIATED WITH Neurodevelopmental Disorders; Polyarteritis Nodosa, Childhood-Onset; INTERACTS WITH aflatoxin B2
Type: ncrna
RefSeq Status: VALIDATED
Also known as: cat eye syndrome chromosome region, candidate 3 (non-protein coding)
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl2217,256,859 - 17,266,733 (-)EnsemblGRCh38hg38GRCh38
GRCh382217,256,859 - 17,266,733 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh372217,737,749 - 17,747,623 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 342216,112,302 - 16,122,177NCBI
Cytogenetic Map22q11.1NCBI
HuRef221,556,219 - 1,566,089 (-)NCBIHuRef
CHM1_12217,742,208 - 17,752,082 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction 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 CECR3
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1346490
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2020-08-04
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.