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Gene: SNORD115-26 (small nucleolar RNA, C/D box 115-26) Homo sapiens
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Symbol: SNORD115-26
Name: small nucleolar RNA, C/D box 115-26
Description: ASSOCIATED WITH Angelman syndrome; autistic disorder; schizophrenia; INTERACTS WITH cadmium atom; valproic acid
Type: snorna
RefSeq Status: VALIDATED
Also known as: HBII-52-26
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381525,218,617 - 25,218,698 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371525,463,764 - 25,463,845 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361523,014,857 - 23,014,938 (+)NCBINCBI36hg18NCBI36
Celera153,625,788 - 3,625,869 (+)NCBI
Cytogenetic Map15q11.2NCBI
HuRef153,588,248 - 3,588,329 (+)NCBIHuRef
CHM1_11525,413,278 - 25,413,359 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - curated
References - uncurated

Genomics

miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on SNORD115-26
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1606611
Created: 2007-04-29
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.