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Gene: SNORD116-11 (small nucleolar RNA, C/D box 116-11) Homo sapiens
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Symbol: SNORD116-11
Name: small nucleolar RNA, C/D box 116-11
Description: ASSOCIATED WITH Angelman syndrome; autistic disorder; schizophrenia; INTERACTS WITH 2-hydroxypropanoic acid; dioxygen; rac-lactic acid
Type: snorna
RefSeq Status: VALIDATED
Also known as: HBII-85-11
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl1525,075,929 - 25,076,020 (+)Ensembl
GRCh381525,075,928 - 25,076,021 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371525,321,075 - 25,321,168 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361522,872,168 - 22,872,261 (+)NCBINCBI36hg18NCBI36
Celera153,483,046 - 3,483,139 (+)NCBI
Cytogenetic Map15q11.2NCBI
HuRef153,456,933 - 3,457,026 (+)NCBIHuRef
CHM1_11525,270,595 - 25,270,688 (+)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

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on SNORD116-11
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1604107
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.