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Gene: AP000289.1 (novel transcript) Homo sapiens
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Symbol: AP000289.1
Name: novel transcript
RGD ID: 16553504
Description:
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LOC101928107; uncharacterized LOC101928107
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38.p13 Ensembl - Human Genome Assembly GRCh38 Ensembl
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl2133,110,867 - 33,123,725 (-)EnsemblGRCh38hg38GRCh38
GRCh382133,111,704 - 33,123,700 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh372134,484,010 - 34,496,006 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map21q22.11NCBI
CHM1_12134,046,103 - 34,058,099 (-)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 AP000289.1
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 16553504
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.