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Gene: RB1-DT (RB1 divergent transcript) Homo sapiens
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Symbol: RB1-DT
Name: RB1 divergent transcript
Description: ASSOCIATED WITH Chromosome 13q Deletion Syndrome; chromosome 13q14 deletion syndrome; INTERACTS WITH dorsomorphin; methylmercury chloride; SB 431542
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LINC00441; long intergenic non-protein coding RNA 441; ncRNA-RB1; RP11-305D15.2
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381348,296,513 - 48,303,702 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371348,870,649 - 48,877,797 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map13q14.2NCBI
HuRef1329,662,878 - 29,670,058 (-)NCBIHuRef
CHM1_11348,838,376 - 48,845,511 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Genomics

miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on RB1-DT
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 5688842
Created: 2012-03-06
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.