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Gene: LINCR-0001 (uncharacterized LINCR-0001) Homo sapiens
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Symbol: LINCR-0001
Name: uncharacterized LINCR-0001
CRRD ID: 16559858
Description:
Type: ncrna
RefSeq Status: VALIDATED
Also known as: AC104964.1; novel transcript
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38.p13 Ensembl - Human Genome Assembly GRCh38 Ensembl
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl810,474,565 - 10,482,388 (+)EnsemblGRCh38hg38GRCh38
GRCh38810,474,565 - 10,481,974 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37810,330,932 - 10,335,373 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map8p23.1NCBI
HuRef89,261,465 - 9,265,929 (+)NCBIHuRef
CHM1_1810,397,852 - 10,405,246 (+)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 LINCR-0001
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 16559858
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.