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Gene: AC104024.1 (novel transcript) Homo sapiens
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Symbol: AC104024.1
Name: novel transcript
RGD ID: 16554811
Description: ASSOCIATED WITH autistic disorder
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LOC284191; uncharacterized LOC284191
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38.p13 Ensembl - Human Genome Assembly GRCh38 Ensembl
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1716,975,999 - 16,981,353 (-)EnsemblGRCh38hg38GRCh38
GRCh381716,975,999 - 16,981,353 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371716,879,313 - 16,884,667 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map17p11.2NCBI
HuRef1716,632,309 - 16,637,680 (-)NCBIHuRef
CHM1_11716,888,260 - 16,894,344 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - uncurated

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on AC104024.1
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 16554811
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.