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Gene: PWRN3 (Prader-Willi region non-protein coding RNA 3) Homo sapiens
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Symbol: PWRN3
Name: Prader-Willi region non-protein coding RNA 3
Description: ASSOCIATED WITH autistic disorder; schizophrenia
Type: ncrna
RefSeq Status: VALIDATED
Also known as: RP11-580I1.3
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381524,441,127 - 24,447,967 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371524,689,647 - 24,696,951 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map15q11.2NCBI
HuRef152,825,382 - 2,832,682 (+)NCBIHuRef
CHM1_11524,635,859 - 24,642,699 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - uncurated

Genomics


Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on PWRN3
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 7338743
Created: 2013-09-17
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.