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Gene: CDKN2A-DT (CDKN2A divergent transcript) Homo sapiens
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Symbol: CDKN2A-DT
Name: CDKN2A divergent transcript
Description: ASSOCIATED WITH familial melanoma; schizophrenia; INTERACTS WITH copper(II) sulfate
Type: ncrna
RefSeq Status: VALIDATED
Also known as: bA149I2.3; C9orf53; CDKN2A antisense RNA 1 (head to head); CDKN2A-AS1
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38921,967,139 - 21,967,754 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37921,967,138 - 21,967,753 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36921,957,199 - 21,957,752 (+)NCBINCBI36hg18NCBI36
Celera921,905,490 - 21,906,105 (+)NCBI
Cytogenetic Map9p21.3NCBI
HuRef921,930,287 - 21,930,971 (+)NCBIHuRef
CHM1_1921,967,033 - 21,967,648 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Genomics

Position Markers

Expression


Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on CDKN2A-DT
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1347500
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2019-12-03
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.