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Gene: AL117329.1 (novel transcript) Homo sapiens
Analyze
Symbol: AL117329.1
Name: novel transcript
Description:
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LOC284930; uncharacterized LOC284930
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38.p13 Ensembl - Human Genome Assembly GRCh38 Ensembl
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl2247,630,827 - 48,023,004 (+)EnsemblGRCh38hg38GRCh38
GRCh382247,631,674 - 47,855,600 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh372248,027,452 - 48,251,349 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map22q13.31NCBI
HuRef2230,974,486 - 31,198,402 (+)NCBIHuRef
CHM1_12247,986,179 - 48,210,541 (+)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 AL117329.1
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 16552835
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.