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Gene: VSTM2A-OT1 (VSTM2A overlapping transcript 1) Homo sapiens
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Symbol: VSTM2A-OT1
Name: VSTM2A overlapping transcript 1
Description: ASSOCIATED WITH autistic disorder
Type: ncrna
RefSeq Status: VALIDATED
Also known as: GS1-18A18.1
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl754,556,970 - 54,571,726 (+)EnsemblGRCh38hg38GRCh38
GRCh38754,556,970 - 54,571,726 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37754,624,663 - 54,639,419 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map7p11.2NCBI
HuRef754,461,699 - 54,476,415 (+)NCBIHuRef
CHM1_1754,627,184 - 54,641,907 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - curated
References - uncurated

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on VSTM2A-OT1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 8662669
Created: 2014-06-24
Species: Homo sapiens
Last Modified: 2020-03-24
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.