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Gene: PWAR4 (Prader Willi/Angelman region RNA 4) Homo sapiens
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Symbol: PWAR4
Name: Prader Willi/Angelman region RNA 4
Description: ASSOCIATED WITH Angelman syndrome; autism spectrum disorder; autistic disorder; INTERACTS WITH aflatoxin B2; benzo[a]pyrene; valproic acid
Type: ncrna
RefSeq Status: VALIDATED
Also known as: PAR-4; PAR4
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381525,211,692 - 25,212,033 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371525,456,839 - 25,457,180 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361523,007,932 - 23,008,269 (+)NCBINCBI36hg18NCBI36
Celera153,618,863 - 3,619,204 (+)NCBI
Cytogenetic Map15q11.2NCBI
HuRef153,581,323 - 3,581,664 (+)NCBIHuRef
CHM1_11525,406,353 - 25,406,694 (+)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 PWAR4
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 7249560
Created: 2013-08-20
Species: Homo sapiens
Last Modified: 2020-03-24
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.