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Gene: AL357507.1 (novel transcript) Homo sapiens
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Symbol: AL357507.1
Name: novel transcript
Description:
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LOC101928516; uncharacterized LOC101928516
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38.p13 Ensembl - Human Genome Assembly GRCh38 Ensembl
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl674,069,451 - 74,690,727 (+)EnsemblGRCh38hg38GRCh38
GRCh38674,069,451 - 74,690,727 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37674,779,167 - 75,400,443 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map6q13NCBI
HuRef671,979,208 - 72,599,051 (+)NCBIHuRef
CHM1_1674,934,998 - 75,566,969 (+)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 AL357507.1
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 16552691
Created: 2020-01-08
Species: Homo sapiens
Last Modified: 2020-08-04
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.