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Gene: AP001042.3 (novel transcript) Homo sapiens
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Symbol: AP001042.3
Name: novel transcript
RGD ID: 16572176
Description:
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LOC101928398; uncharacterized LOC101928398
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38.p13 Ensembl - Human Genome Assembly GRCh38 Ensembl
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl2138,857,539 - 38,858,861 (+)EnsemblGRCh38hg38GRCh38
GRCh382138,857,539 - 38,858,862 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh372140,229,282 - 40,230,785 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map21q22.2NCBI
HuRef2125,699,374 - 25,700,877 (+)NCBIHuRef
CHM1_12139,790,061 - 39,791,384 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model



Genomics


Expression


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on AP001042.3
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 16572176
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.