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Gene: PWAR5 (Prader Willi/Angelman region RNA 5) Homo sapiens
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Symbol: PWAR5
Name: Prader Willi/Angelman region RNA 5
Description: ASSOCIATED WITH Angelman syndrome; autism spectrum disorder; autistic disorder; INTERACTS WITH 17beta-estradiol; aflatoxin B1; chromium(6+)
Type: ncrna
RefSeq Status: VALIDATED
Also known as: D15S226E; PAR-5; PAR5
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381524,984,860 - 24,988,232 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371525,230,007 - 25,233,379 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361522,781,293 - 22,784,474 (+)NCBINCBI36hg18NCBI36
Celera153,392,000 - 3,395,372 (+)NCBI
Cytogenetic Map15q11.2NCBI
HuRef153,365,927 - 3,369,299 (+)NCBIHuRef
CHM1_11525,179,549 - 25,182,921 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Genomics


Expression


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on PWAR5
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 7246117
Created: 2013-06-18
Species: Homo sapiens
Last Modified: 2019-10-16
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.