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Gene: AC246817.1 (novel transcript) Homo sapiens
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Symbol: AC246817.1
Name: novel transcript
Description: ASSOCIATED WITH schizophrenia
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LOC105377785; uncharacterized LOC105377785
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38.p13 Ensembl - Human Genome Assembly GRCh38 Ensembl
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl82,726,956 - 2,838,823 (+)EnsemblGRCh38hg38GRCh38
GRCh38.p13 Ensembl82,726,956 - 2,926,689 (+)EnsemblGRCh38hg38GRCh38
GRCh3882,726,956 - 3,024,231 (+)NCBIGRCh38GRCh38hg38GRCh38
Cytogenetic Map8p23.2NCBI
CHM1_182,739,853 - 2,787,029 (+)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 AC246817.1
NCBI Gene
Ensembl Gene
JBrowse: hg38
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 16559969
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.