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Gene: SNORD115-16 (small nucleolar RNA, C/D box 115-16) Homo sapiens
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Symbol: SNORD115-16
Name: small nucleolar RNA, C/D box 115-16
Description: ASSOCIATED WITH Angelman syndrome; autistic disorder; schizophrenia; INTERACTS WITH valproic acid
Type: snorna
RefSeq Status: VALIDATED
Also known as: HBII-52-16
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381525,199,448 - 25,199,529 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371525,444,595 - 25,444,676 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361522,995,688 - 22,995,769 (+)NCBINCBI36hg18NCBI36
Celera153,606,607 - 3,606,688 (+)NCBI
Cytogenetic Map15q11.2NCBI
HuRef153,569,071 - 3,569,152 (+)NCBIHuRef
CHM1_11525,394,109 - 25,394,190 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - uncurated

Genomics

miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on SNORD115-16
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1604077
Created: 2007-04-28
Species: Homo sapiens
Last Modified: 2019-10-16
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.