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Gene: SNORD116@ (small nucleolar RNA, C/D box 116 cluster) Homo sapiens
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Symbol: SNORD116@
Name: small nucleolar RNA, C/D box 116 cluster
CRRD ID: 1342546
Description: ASSOCIATED WITH Angelman syndrome; autistic disorder; schizophrenia; INTERACTS WITH 2-hydroxypropanoic acid; entinostat; rac-lactic acid
Type: gene
RefSeq Status: VALIDATED
Also known as: HBII-85; PET1; Prader-Willi syndrome chromosome region 1; PWCR1
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381525,051,476 - 25,106,603 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371525,296,623 - 25,351,750 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361522,847,716 - 22,902,843 (+)NCBINCBI36hg18NCBI36
Build 341522,883,900 - 22,885,135NCBI
Celera153,458,596 - 3,513,721 (+)NCBI
Cytogenetic Map15q11.2NCBI
HuRef153,432,481 - 3,487,638 (+)NCBIHuRef
CHM1_11525,246,150 - 25,301,268 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Genomics


Expression


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on SNORD116@
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1342546
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2020-09-16
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.