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Gene: AC100810.1 (novel transcript) Homo sapiens
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Symbol: AC100810.1
Name: novel transcript
Description: ASSOCIATED WITH neuronal ceroid lipofuscinosis; neuronal ceroid lipofuscinosis 8
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LOC101927752; uncharacterized LOC101927752
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38.p13 Ensembl - Human Genome Assembly GRCh38 Ensembl
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl81,761,054 - 1,764,508 (-)EnsemblGRCh38hg38GRCh38
GRCh3881,761,963 - 1,764,584 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh3781,710,788 - 1,711,500 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map8p23.3NCBI
HuRef81,525,516 - 1,526,228 (-)NCBIHuRef
CHM1_181,709,816 - 1,712,448 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on AC100810.1
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 16560032
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.