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Gene: AC068587.4 (novel transcript) Homo sapiens
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Symbol: AC068587.4
Name: novel transcript
CRRD ID: 16570333
Description:
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LOC729732; uncharacterized LOC729732
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38.p13 Ensembl - Human Genome Assembly GRCh38 Ensembl
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl812,467,693 - 12,665,588 (-)EnsemblGRCh38hg38GRCh38
GRCh38812,537,079 - 12,665,611 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37812,394,588 - 12,523,120 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map8p23.1NCBI
HuRef811,059,456 - 11,065,753 (-)NCBIHuRef
CHM1_1812,596,197 - 12,724,656 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - curated
References - uncurated

Genomics


Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on AC068587.4
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 16570333
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.