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Gene: OPA1-AS1 (OPA1 antisense RNA 1) Homo sapiens
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Symbol: OPA1-AS1
Name: OPA1 antisense RNA 1
Description: ASSOCIATED WITH Behr Syndrome; dominant optic atrophy plus syndrome; mitochondrial DNA depletion syndrome 14
Type: ncrna
RefSeq Status: VALIDATED
Also known as: RP11-175P19.1
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl3193,618,609 - 193,627,337 (-)Ensembl
GRCh383193,618,599 - 193,627,332 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh373193,336,388 - 193,345,121 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map3q29NCBI
HuRef3190,723,546 - 190,732,276 (-)NCBIHuRef
CHM1_13193,299,212 - 193,308,005 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - curated
References - uncurated

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on OPA1-AS1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 6481413
Created: 2012-04-10
Species: Homo sapiens
Last Modified: 2020-01-14
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.