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Gene: AC139887.2 (novel transcript, antisense to PCGF3) Homo sapiens
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Symbol: AC139887.2
Name: novel transcript, antisense to PCGF3
Description:
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LOC100129917; uncharacterized LOC100129917
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38.p13 Ensembl - Human Genome Assembly GRCh38 Ensembl
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl4760,202 - 781,859 (-)EnsemblGRCh38hg38GRCh38
GRCh384780,149 - 781,848 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh374773,937 - 775,636 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map4p16.3NCBI
HuRef4744,720 - 746,418 (-)NCBIHuRef
CHM1_14770,885 - 772,584 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


References - uncurated

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on AC139887.2
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 16558549
Created: 2020-01-08
Species: Homo sapiens
Last Modified: 2020-06-18
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.