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Gene: MYCBP2-AS1 (MYCBP2 antisense RNA 1) Homo sapiens
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Symbol: MYCBP2-AS1
Name: MYCBP2 antisense RNA 1
Description: ASSOCIATED WITH Chromosome 13q Deletion Syndrome; chromosome 13q14 deletion syndrome; INTERACTS WITH 2-hydroxypropanoic acid; rac-lactic acid; triclosan
Type: ncrna
RefSeq Status: VALIDATED
Also known as: RP11-226E21.3
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381377,075,514 - 77,087,776 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371377,649,649 - 77,661,911 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map13q22.3NCBI
HuRef1358,347,369 - 58,359,631 (+)NCBIHuRef
CHM1_11377,617,540 - 77,629,802 (+)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 MYCBP2-AS1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 6481169
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.