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Gene: PICSAR (P38 inhibited cutaneous squamous cell carcinoma associated lincRNA) Homo sapiens
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Symbol: PICSAR
Name: P38 inhibited cutaneous squamous cell carcinoma associated lincRNA
Description: ASSOCIATED WITH autistic disorder
Type: ncrna
RefSeq Status: VALIDATED
Also known as: C21orf113; LINC00162; long intergenic non-protein coding RNA 162; NCRNA00162; NLC1-C; NLC1C; PRED74
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382144,999,208 - 45,004,727 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh372146,419,126 - 46,424,642 (-)NCBIGRCh37GRCh37hg19GRCh37
Celera2131,525,732 - 31,531,284 (-)NCBI
Cytogenetic Map21q22.3NCBI
HuRef2131,792,858 - 31,798,382 (-)NCBIHuRef
CHM1_12145,979,972 - 45,985,494 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - uncurated

Genomics


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

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

RGD Object Information
RGD ID: 1345871
Created: 2005-03-08
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.