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Gene: AL133464.1 (novel transcript) Homo sapiens
Analyze
Symbol: AL133464.1
Name: novel transcript
Description:
Type: ncrna
RefSeq Status: PREDICTED
Also known as: LOC284788; uncharacterized LOC284788
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38.p13 Ensembl - Human Genome Assembly GRCh38 Ensembl
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl2022,371,216 - 22,471,557 (-)EnsemblGRCh38hg38GRCh38
GRCh382022,400,333 - 22,420,643 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh372022,380,971 - 22,401,281 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map20p11.21NCBI
HuRef2022,343,773 - 22,364,083 (-)NCBIHuRef
CHM1_12022,381,407 - 22,401,715 (-)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 AL133464.1
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 16551552
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.