Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   
Gene: AC116565.1 (novel transcript) Homo sapiens
Analyze
Symbol: AC116565.1
Name: novel transcript
Description:
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LOC105374338; uncharacterized LOC105374338
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38.p13 Ensembl - Human Genome Assembly GRCh38 Ensembl
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl4577,168 - 618,076 (+)EnsemblGRCh38hg38GRCh38
GRCh384577,168 - 584,866 (+)NCBIGRCh38GRCh38hg38GRCh38
Cytogenetic Map4p16.3NCBI
CHM1_14570,514 - 578,016 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


References - uncurated

Genomics


Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on AC116565.1
NCBI Gene
Ensembl Gene
JBrowse: hg38
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 16570161
Created: 2020-01-08
Species: Homo sapiens
Last Modified: 2020-06-18
Status: ACTIVE



NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.