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Gene: PDE6B-AS1 (PDE6B antisense RNA 1) Homo sapiens
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Symbol: PDE6B-AS1
Name: PDE6B antisense RNA 1
Description: ASSOCIATED WITH congenital stationary night blindness autosomal dominant 2; fundus dystrophy; retinitis pigmentosa
Type: ncrna
RefSeq Status: MODEL
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl4652,850 - 656,213 (-)EnsemblGRCh38hg38GRCh38
GRCh384652,909 - 656,188 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh374647,012 - 649,500 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map4p16.3NCBI
HuRef4622,177 - 624,665 (-)NCBIHuRef
CHM1_14646,486 - 649,765 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - uncurated

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on PDE6B-AS1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 14974459
Created: 2019-09-24
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.