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Gene: AP001107.9 (novel transcript, antisense to SLC29A2) Homo sapiens
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Symbol: AP001107.9
Name: novel transcript, antisense to SLC29A2
RGD ID: 16560771
Description:
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LOC102724064; uncharacterized LOC102724064
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38.p13 Ensembl - Human Genome Assembly GRCh38 Ensembl
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1166,347,950 - 66,364,804 (+)EnsemblGRCh38hg38GRCh38
GRCh381166,347,991 - 66,363,764 (+)NCBIGRCh38GRCh38hg38GRCh38
Cytogenetic Map11q13.2NCBI
CHM1_11165,999,532 - 66,015,307 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


References - uncurated

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on AP001107.9
NCBI Gene
Ensembl Gene
JBrowse: hg38
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 16560771
Created: 2020-01-08
Species: Homo sapiens
Last Modified: 2020-09-16
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.