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Gene: SNORD116-19 (small nucleolar RNA, C/D box 116-19) Homo sapiens
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Symbol: SNORD116-19
Name: small nucleolar RNA, C/D box 116-19
Description: ASSOCIATED WITH Angelman syndrome; autistic disorder; schizophrenia
Type: snorna
RefSeq Status: VALIDATED
Also known as: HBII-85-19
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381525,086,526 - 25,086,619 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371525,331,673 - 25,331,765 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361522,882,766 - 22,882,859 (+)NCBINCBI36hg18NCBI36
Celera153,493,644 - 3,493,737 (+)NCBI
Cytogenetic Map15q11.2NCBI
HuRef153,467,531 - 3,467,623 (+)NCBIHuRef
CHM1_11525,281,193 - 25,281,286 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - curated
References - uncurated

Genomics

Position Markers
miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on SNORD116-19
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1604119
Created: 2007-04-28
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.