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Gene: SNORD116-26 (small nucleolar RNA, C/D box 116-26) Homo sapiens
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Symbol: SNORD116-26
Name: small nucleolar RNA, C/D box 116-26
Description: ASSOCIATED WITH Angelman syndrome; autistic disorder; schizophrenia
Type: snorna
RefSeq Status: VALIDATED
Also known as: HBII-85-26
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl1525,099,499 - 25,099,594 (+)Ensembl
GRCh381525,099,498 - 25,099,595 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371525,344,645 - 25,344,742 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361522,895,738 - 22,895,835 (+)NCBINCBI36hg18NCBI36
Celera153,506,615 - 3,506,712 (+)NCBI
Cytogenetic Map15q11.2NCBI
HuRef153,480,532 - 3,480,629 (+)NCBIHuRef
CHM1_11525,294,162 - 25,294,259 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - uncurated

Genomics

Position Markers
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on SNORD116-26
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1604092
Created: 2007-04-28
Species: Homo sapiens
Last Modified: 2019-12-25
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.