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Gene: SNORD116-29 (small nucleolar RNA, C/D box 116-29) Homo sapiens
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Symbol: SNORD116-29
Name: small nucleolar RNA, C/D box 116-29
Description: ASSOCIATED WITH Angelman syndrome; autistic disorder; schizophrenia; INTERACTS WITH sodium arsenite
Type: snorna
RefSeq Status: VALIDATED
Also known as: HBII-85-29
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl1525,106,521 - 25,106,603 (+)Ensembl
GRCh381525,106,520 - 25,106,604 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371525,351,667 - 25,351,751 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361522,902,760 - 22,902,844 (+)NCBINCBI36hg18NCBI36
Celera153,513,638 - 3,513,722 (+)NCBI
Cytogenetic Map15q11.2NCBI
HuRef153,487,555 - 3,487,639 (+)NCBIHuRef
CHM1_11525,301,185 - 25,301,269 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - uncurated

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on SNORD116-29
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1606593
Created: 2007-04-29
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.